US10065157B2 - Mixer and processes incorporating the same - Google Patents
Mixer and processes incorporating the same Download PDFInfo
- Publication number
- US10065157B2 US10065157B2 US14/436,604 US201314436604A US10065157B2 US 10065157 B2 US10065157 B2 US 10065157B2 US 201314436604 A US201314436604 A US 201314436604A US 10065157 B2 US10065157 B2 US 10065157B2
- Authority
- US
- United States
- Prior art keywords
- chamber
- mixer
- inner diameter
- zone
- inlet
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Fee Related, expires
Links
Images
Classifications
-
- B01F5/0653—
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01F—MIXING, e.g. DISSOLVING, EMULSIFYING OR DISPERSING
- B01F25/00—Flow mixers; Mixers for falling materials, e.g. solid particles
- B01F25/40—Static mixers
- B01F25/42—Static mixers in which the mixing is affected by moving the components jointly in changing directions, e.g. in tubes provided with baffles or obstructions
- B01F25/43—Mixing tubes, e.g. wherein the material is moved in a radial or partly reversed direction
- B01F25/433—Mixing tubes wherein the shape of the tube influences the mixing, e.g. mixing tubes with varying cross-section or provided with inwardly extending profiles
- B01F25/4335—Mixers with a converging-diverging cross-section
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01F—MIXING, e.g. DISSOLVING, EMULSIFYING OR DISPERSING
- B01F25/00—Flow mixers; Mixers for falling materials, e.g. solid particles
- B01F25/40—Static mixers
- B01F25/42—Static mixers in which the mixing is affected by moving the components jointly in changing directions, e.g. in tubes provided with baffles or obstructions
- B01F25/43—Mixing tubes, e.g. wherein the material is moved in a radial or partly reversed direction
- B01F25/433—Mixing tubes wherein the shape of the tube influences the mixing, e.g. mixing tubes with varying cross-section or provided with inwardly extending profiles
- B01F25/4336—Mixers with a diverging cross-section
-
- B01F5/0652—
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J19/00—Chemical, physical or physico-chemical processes in general; Their relevant apparatus
- B01J19/24—Stationary reactors without moving elements inside
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J4/00—Feed or outlet devices; Feed or outlet control devices
- B01J4/001—Feed or outlet devices as such, e.g. feeding tubes
- B01J4/002—Nozzle-type elements
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C17/00—Preparation of halogenated hydrocarbons
- C07C17/013—Preparation of halogenated hydrocarbons by addition of halogens
- C07C17/04—Preparation of halogenated hydrocarbons by addition of halogens to unsaturated halogenated hydrocarbons
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01F—MIXING, e.g. DISSOLVING, EMULSIFYING OR DISPERSING
- B01F25/00—Flow mixers; Mixers for falling materials, e.g. solid particles
- B01F25/10—Mixing by creating a vortex flow, e.g. by tangential introduction of flow components
- B01F25/102—Mixing by creating a vortex flow, e.g. by tangential introduction of flow components wherein the vortex is created by two or more jets introduced tangentially in separate mixing chambers or consecutively in the same mixing chamber
-
- B01F5/0062—
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J2219/00—Chemical, physical or physico-chemical processes in general; Their relevant apparatus
- B01J2219/19—Details relating to the geometry of the reactor
- B01J2219/194—Details relating to the geometry of the reactor round
- B01J2219/1941—Details relating to the geometry of the reactor round circular or disk-shaped
- B01J2219/1943—Details relating to the geometry of the reactor round circular or disk-shaped cylindrical
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J2219/00—Chemical, physical or physico-chemical processes in general; Their relevant apparatus
- B01J2219/24—Stationary reactors without moving elements inside
Definitions
- the present invention relates to an efficient and effective mixer, an apparatus comprising the mixer and a reactor, and processes incorporating the same.
- Hydrofluorocarbon (HFC) products are widely utilized in many applications, including refrigeration, air conditioning, foam expansion, and as propellants for aerosol products including medical aerosol devices. Although HFC's have proven to be more climate friendly than the chlorofluorocarbon and hydrochlorofluorocarbon products that they replaced, it has now been discovered that they exhibit an appreciable global warming potential (GWP).
- GWP global warming potential
- HFO hydrofluoroolefin
- HFO cyclopentafluoroprop-1-ene
- a desirable HFO compound e.g., such as 2,3,3,3-tetrafluoroprop-1-ene or 1,3,3,3-tetrafluoroprop-1-ene
- feedstocks of chlorocarbons or chlorofluorocarbons, and in particular, chlorinated propenes may typically be produced utilizing feedstocks of chlorocarbons or chlorofluorocarbons, and in particular, chlorinated propenes.
- chlorinated propenes may have limited commercial availability, and/or may only be available at potentially prohibitively high cost, due at least in part to the propensity of the conventional processes typically utilized in their manufacture to result in the production of large quantities of secondary products, i.e., waste and/or by-products. Any such secondary products produced not only have to be separated from the final product and disposed of, but also, can result in system fouling prior to doing so. Both of these outcomes can introduce substantial expense, further limiting the commercial potential of processes in which the production of such secondary products is not reduced or eliminated. Further, these problems become exacerbated on process scale-up, so that large scale processes can become cost prohibitive quickly.
- mixers have been developed in efforts to minimize backmixing of reactants that may occur prior to entry into the reactor; however, none of these are without detriment.
- mixers have been provided having the same diameter as the reactor so that backmixing zones are not created at the junction there between. When coupled with appropriate introduction of reactants, these mixers have proven effective, but can yet be suboptimal.
- mixers for use in methods wherein limiting reactants are desirably utilized. More particularly, mixers that provide quick and thorough mixing of two or more reactants, while yet also minimizing back mixing of the mixed feed stream and thus providing a reduction in the amount of secondary products that are produced would be welcomed in the art. Further advantage would be seen if such mixers could be provided cost effectively, i.e., on a smaller scale than the reactors with which they are desirably utilized.
- the mixer incorporates an expander zone, wherein the inner diameter thereof expands outwardly at an angle of less than 90° relative to a longitudinal axis of the expander zone.
- a mixer can be provided having an inlet diameter smaller than its exit diameter, so that when coupled to a reactor, any backmixing zone that may otherwise be provided by disparate geometries between the mixer outlet and reactor inlet can be minimized or eliminated.
- the mixer may also incorporate one or more chambers, flow pattern development zones, and/or mixing zones that can act alone or together to improve the flow and/or mixing of the reactants therein so that uniform and efficient mixing is provided by the mixer.
- a mixer comprising at least one inlet to at least one chamber, and an expander zone.
- the angle created by a longitudinal axis of the chamber and a longitudinal axis of the inlet (hereinafter the ‘chamber-inlet angle’, or a in FIG. 1A ) is less than 90°, or may be from 30° to 80°.
- the inner diameter of the expander zone (D e ) expands outwardly at an angle (hereinafter the ‘expander angle’ or ⁇ in FIG. 1A ) less than 90°, or less than 45°, or less than 20°, or less than 15°, or even less than 10° relative to a longitudinal axis of the expander zone.
- the chamber has an inner diameter (D c ) that is at least 1.25, or at least 2 times greater than the inner diameter of its inlet (D ci ). In some embodiments, the inner diameter of the chamber (D c ) may be from 2-10 times greater than the inner diameter of its inlet (D ci ).
- the chamber also desirably comprises an outlet, and in those embodiments wherein multiple chambers/inlets are utilized, the outlets thereof are desirably arranged concentrically, i.e., so that two concentrically placed outlets create an annular space there between.
- the ratio of the cross sectional area of each annular space (A a ) to the area of the inner most chamber outlet (A co , innermost) is desirably between 1 and 3, i.e., A a /A co is between 1 and 3.
- the chamber inner diameter (D c ) may taper to the inner diameter of the chamber outlet (D co ), or, the chamber inner diameter (D c ) may decrease at a 90° angle to provide the chamber outlet.
- the chamber outlet has an inner diameter (D co ) that is at least 2 times greater than the inner diameter of the chamber inlet (D ci ).
- the outlet has an inner diameter (D co ) that is less than the chamber inner diameter (D c ), e.g., the ratio of the chamber inner diameter (D c ) to the outlet inner diameter (D co ) may be at least 1, or at least 1.1, or at least 1.2. Desirably, the ratio of the inner diameter of the chamber (D c ) to the inner diameter of its outlet (D co ) is less than 10, or less than 8, or less than 6, or less than 5, or less than 4.
- the ratio of the inner diameter of the chamber (D c ) to the inner diameter of its outlet (D co ) is from 1.1 to 8 or from 1.2-4. In some embodiments, the inner diameter of the chamber (D c ) and the inner diameter of its outlet (D co ) may be approximately the same.
- the mixer may additionally comprise a flow pattern development zone and/or a mixing zone.
- the flow pattern development zone may be an extension of the chamber outlet(s), i.e., may be a series of concentrically placed tubes creating an inner tube and a series of annular spaces.
- the length of any flow pattern development zone (L fpd ) may desirably be substantially the same as, or greater than, the diameter of the outermost tube (D fpd ) within the flow development zone. If both a mixing zone and a flow pattern development zone are utilized, the mixing zone is desirably downstream of the flow pattern development zone.
- the mixing zone may desirably comprise a single tube having an inner diameter (D m ) less than or equal to that of the outermost chamber outlet (D co , outermost), or the outermost tube of the flow pattern development zone (D fpd ), as the case may be.
- the combined mixing zone and flow pattern development zone if any, has a length (L fpd +L m ) 3 times greater, or 9 times greater, than the inner diameter (D m ) of the mixing zone.
- an apparatus comprising a reactor having an inlet with an inner diameter (D r ) and a mixer comprising at least one inlet to at least one chamber, wherein the chamber outlet inner diameter (D co ), flow pattern development zone inner diameter (D fpd ) and/or mixing zone inner diameter (D m ) is/are less than that of the reactor inlet inner diameter (D r ).
- the ratio of the inner diameter of the reactor (D r ) to the chamber outlet inner diameter (D cp ), flow pattern development zone inner diameter (D fpd ) and/or mixing zone inner diameter (D m ) is desirably from 2 to 5, or from 3 to 4.
- the mixer also comprises an expander zone having an inner diameter (D e ) that expands outwardly at an angle of less than 90°, or less than 45°, or less than 20°, or less than 10°.
- the reactor may have an inner diameter of more or less than 4 feet.
- the reactor and/or mixer may comprise one or more bends of 90 degrees or greater, to accommodate the desired design and length thereof easily in the available manufacturing space.
- processes for mixing at least two reagents for a chemical process comprise providing the at least two reactants to an apparatus comprising a reactor having an inner diameter (D r ) and a mixer comprising at least one inlet to at least one chamber, wherein the chamber outlet inner diameter (D co ), flow pattern development zone inner diameter (D fpd ) and/or mixing zone inner diameter (D m ) is/are less than that of the reactor inlet inner diameter (D r ).
- the ratio the inner diameter of the reactor (D r ) to the outermost chamber outlet inner diameter D co and/or the mixing zone inner diameter (D m ) is desirably from 2 to 6, or from 3 to 5.
- the mixer also comprises an expander zone having an inner diameter (D e ) that expands outwardly at an angle of less than 90°, or less than 45°, or less than 20°, or less than 10°.
- FIG. 1A is a schematic representation (not to scale) of one embodiment of the mixer comprising one inlet/chamber and an expander zone;
- FIG. 1B is a top view of the schematic representation of the embodiment shown in FIG. 1A ;
- FIG. 1C is a schematic representation (not to scale) of the mixer shown in FIG. 1 , further comprising a taper from the chamber inner diameter to provide the chamber outlet;
- FIG. 2A is a schematic representation (not to scale) of one embodiment of the mixer comprising two inlets/chambers and an expander zone;
- FIG. 2B is a top view of one arrangement of the chamber inlets of the embodiment shown in FIG. 2A ;
- FIG. 2C is a top view of a further arrangement of the chamber inlets of the embodiment shown in FIG. 2A ;
- FIG. 3A is a schematic representation (not to scale) of one embodiment of the mixer comprising two inlets/chambers, a mixing zone and an expander zone;
- FIG. 3B is a schematic representation (not to scale) of one embodiment of the mixer comprising two inlets/chambers, a flow pattern development zone and an expander zone;
- FIG. 3C is a schematic representation (not to scale) of one embodiment of the mixer comprising two inlets/chambers, a flow pattern development zone, a mixing zone and an expander zone;
- FIG. 4A is a schematic representation (not to scale) of one embodiment of the mixer comprising three inlets and two chambers, a flow pattern development zone, a mixing zone and an expander zone, wherein two inlets are provided on one chamber;
- FIG. 4B is a schematic representation (not to scale) of one embodiment of the mixer comprising three inlets/chambers, a flow pattern development zone, a mixing zone and an expander zone, wherein a third chamber is provided within the second chamber; and
- FIG. 4C is a schematic representation (not to scale) of one embodiment of the mixer comprising three inlets/chambers, a flow pattern development zone, a mixing zone and an expander zone, wherein a third chamber and corresponding inlet is provided between the flow pattern development zone and the mixing zone.
- FIG. 5A shows results of a computational fluid dynamic simulation for a mixer according to one embodiment, having two inlets/chambers, a flow pattern development zone, a mixing zone and an expander zone;
- FIG. 5B shows results of a computational fluid dynamic simulation for a mixer according to one embodiment, having one inlet/chamber, a flow pattern development zone, a mixing zone and an expander zone.
- first”, “second”, and the like, as used herein do not denote any order, quantity, or importance, but rather are used to distinguish one element from another.
- the terms “a” and “an” do not denote a limitation of quantity, but rather denote the presence of at least one of the referenced item, and the terms “front”, “back”, “bottom”, and/or “top”, unless otherwise noted, are merely used for convenience of description, and are not intended to limit the part being described limited to any one position or spatial orientation.
- ranges are inclusive and independently combinable (e.g., ranges of “up to 25 wt. %, or, more specifically, 5 wt. % to 20 wt. %,” is inclusive of the endpoints and all intermediate values of the ranges of “5 wt. % to 25 wt. %,” etc.).
- percent (%) conversion is meant to indicate change in molar or mass flow of reactant in a reactor in ratio to the incoming flow
- percent (%) selectivity means the change in molar flow rate of product in a reactor in ratio to the change of molar flow rate of a reactant.
- the mixer provided herein may incorporate one or more angles between components, zones, or longitudinal axes thereof that provide the mixer with improved performance relative to mixers not incorporating the angle.
- the angles are defined as the lesser angle of the linear pair created by, or that would be created by, the intersection of the components, zones, or axes.
- the chamber-inlet angle (denoted “ ⁇ ” in FIG. 1A ) is defined as the lesser angle of the linear pair created by the intersection of the longitudinal axes of the chamber and the longitudinal axes of its inlet.
- the expander angle (denoted “ ⁇ ” in FIG.
- the transverse chamber-inlet angle (denoted “ ⁇ ” in FIG. 1B ) is defined as the lesser angle of the linear pair created by the intersection of the longitudinal axis of the inlet and a line tangential to the chamber projected on a cross sectional plane to the chamber intersecting the point where the longitudinal axis of the inlet line meets the chamber's wall.
- the present invention provides a mixer for use in a gas-phase process, such as processes for the production of chlorinated propenes and/or higher alkenes.
- the mixer incorporates one or more design features that can i) provide for reduced backmixing of the reactants, and/or ii) minimize or eliminate plugging within the mixer. As a result, desired conversions may be substantially maintained, formation of secondary products may be minimized and/or fouling may be reduced or eliminated. Further, the advantages provided by one design feature may be leveraged, perhaps even synergistically, by combining the same with others.
- the mixer comprises an inlet fluidly connected to a chamber, wherein the chamber-inlet angle ( ⁇ ) is less than 90°.
- the chamber-inlet angle, ⁇ is less than 15°, or less than 80°.
- the chamber-inlet angle ( ⁇ ) may be greater than 20°, or greater than 30°.
- the chamber-inlet angle ( ⁇ ) may be from 30°-80°.
- the mixer also comprises an expander zone, wherein the inner diameter thereof expands outwardly along the length thereof at an expander angle ( ⁇ ) of less than 90°, or less than 45°, or less than 20°, or less than 15°, or less than 10°.
- expander angle ⁇ is greater than 1°, or greater than 2°, or greater than 3°, or greater than 4°, or greater than 5°. In some embodiments, expander angle ⁇ may be from 1° to 90°, or from 2° to 45°, or from 3° to 20°, or from 4° to 15°, or from 5° to 10°.
- the expander may have an inner diameter (D e ) of less than 100 feet, or less than 80 feet, or less than 50 feet, or less than 20 feet. In some embodiments, the expander zone outlet inner diameter (D e ) may be substantially equal to the reactor inlet inner diameter (D r )
- the chamber may exhibit substantially the same geometry as the inlet, and the geometries thereof may be selected to encourage a desired flow pattern. Any flow pattern can be established and encouraged by the mixer (with the exception of back mixed flow).
- the mixer is desirably utilized to produce a swirling flow pattern. Swirling flow patterns can be advantageous for use in many chemical processes, but in particular in processes where backmixing can be an issue. This is because swirling flow patterns tend to produce high shear at internal surfaces that can assist in the prevention of the accumulation of solids thereon. Swirling flow patterns may also only require a small head mixing chamber in comparison to the reactor diameter in order to be established.
- a swirling flow pattern can be induced by introduction of a feedstream into a generally cylindrical inlet, and thereafter into a generally cylindrical chamber.
- the inlet and chamber may have the same, or a different, inner diameter.
- advantage can be seen by providing the chamber with an inner diameter (D c ) at least 1.25 times greater, or at least two times greater, than the inner diameter of the inlet (D ci ).
- the inner diameter of the chamber (D c ) is desirably less than 20 times, or less than 10 times, the inner diameter of the chamber inlet (D ci ).
- the ratio of the inner diameter of the chamber (D c ) to the inner diameter of the inlet (D ci ) is from 2-10.
- the chamber also desirably comprises an outlet, which may desirably be of the same geometry as the chamber and/or inlet.
- the outlet may also have the same diameter, or cross sectional area, as the case may be, as the chamber and/or chamber inlet, or may have a different diameter.
- the chamber outlet has an inner diameter (D co ) that is at least 2 times greater than the inner diameter of the chamber inlet (D ci ).
- the outlet has an inner diameter (D co ) that is less than the chamber inner diameter (D c ), e.g., the ratio of the chamber inner diameter (D c ) to the outlet inner diameter (D co ) may be at least 1, or at least 1.1, or at least 1.2.
- the ratio of the inner diameter of the chamber (D c ) to the inner diameter of its outlet (D co ) is less than 10, or less than 8, or less than 6, or less than 5, or less than 4.
- the ratio of the inner diameter of the chamber (D c ) to the inner diameter of its outlet (D co ) is from 1.1 to 8 or from 1.2-4.
- the outlets of any provided proximate to each other are desirably provided as concentric rings.
- the innermost chamber outlet would act as an egress for one reactant.
- Each subsequent chamber outlet would provide an annular space between it and the chamber outlet immediately interior to it, through which an additional reactant may flow, and so forth.
- the ratio of the cross sectional area of each annular space (A a ) to the area of the inner most chamber outlet (A co , innermost) is desirably between 1 and 3, i.e., A a /A co is between 1 and 3.
- inlet(s)/chamber(s) are provided. In some embodiments, at least two inlets/chambers are provided. In other embodiments, more than one inlet may be provided on one or more chambers. In such embodiments, the additional inlet(s) and/or chamber(s) can have the same configuration, i.e., shape, inner dimension, chamber inlet angle, tangential chamber inlet angle, or one or more different configuration(s). For purposes of manufacturing efficacy, in those embodiments wherein multiple inlets/chambers are used, they may have the same configuration, but this is not necessary to appreciate the advantages of the invention.
- the mixer may be provided with additional features and/or dimensional relationships that further enhance its suitability for use in connection with processes comprising a limiting reagent. More particularly, in some embodiments, the mixer may further comprise an advantageous tangential chamber-inlet angle and/or a flow pattern development zone and/or a mixing zone.
- an angle ⁇ between the chamber inlet and a line tangential to the chamber projected on a cross sectional plane to the chamber intersecting the point where the longitudinal axis of the inlet line meets the chamber's wall of less than 90°, or less than 80°, or less than 70°, or less than 60° provides a beneficial flow to the reactant provided through the inlet.
- the tangential chamber inlet angle ⁇ is greater than 5°, or greater than 10°, or greater than 15°, or greater than 20°.
- the tangential chamber inlet angle ⁇ is from 5° to 90°, or 10° to 80°, or 15° to 70°, or 20° to 60°.
- the flow pattern development zone if provided, will desirably be of a shape and/or dimension that further encourages the formation and/or maintenance of the desired flow pattern of the reactant provided by the at least one inlet.
- the flow pattern development zone may comprise a tube within a tube design, wherein the number of tubes correspond to the number of reactants introduced via inlets/chambers upstream of the flow pattern development zone.
- the flow development zone may simply be a tube having an inner diameter (D fpd ) approximately the same as the inner diameter of the chamber outlet (D co ) and be fluidly connected thereto.
- D fpd inner diameter of the chamber outlet
- D co inner diameter of the chamber outlet
- the innermost tube could be fluidly connected to a first chamber outlet
- the annular space provided between the innermost tube and the next outlying tube could be fluidly connected to a second chamber outlet
- the annular space created by the middle tube and the outermost tube could be fluidly connected to a third chamber outlet.
- two may be introduced via two inlet/chambers, and a third may be introduced according to any method known to those of ordinary skill in the art, and may be introduced, e.g., after a flow pattern development zone.
- This embodiment may be advantageous when a desired reactant has a lesser residence time within the mixer for any reason, e.g., the reactant is highly reactive, unstable at the temperature(s) at which the other reactants are introduced to the mixer, etc.
- a flow pattern development zone in embodiments wherein a flow pattern development zone is desirably included, it can have any suitable length (L fpd ) and inner diameter (D fpd ). Desirably, the length and inner diameter of the flow pattern development zone will facilitate and/or accommodate the desired flow rate of the reactants, while also encouraging or enhancing the desired flow pattern.
- the inner diameter (D fpd ) of the innermost tube of the flow pattern development zone may be greater than 0.25 inch, or greater than 0.5 inch, or greater than 0.75 inches, or greater than 1 inch.
- the inner diameter (D fpd ) of the outermost tube of the flow pattern development zone may be less than 60′′ or less than 30′′ or less than 24′′ or less than 18′′. In some embodiments, the inner diameter (D fpd ) of the innermost tube of the flow pattern development zone is from 0.25 to 60′′ of from 0.5-30′′, or from 0.75 to 24 inches, or from 1′′ to 18′′.
- Any flow pattern development zone can have a length (L fpd ) such that the ratio of its length (L fpd ) to the inner diameter (D fpd ) of the innermost tube thereof is greater than 0.5, or greater than 0.75, or greater than 1.0, or greater than 1.25, or greater than 1.5.
- the ratio L fpd to D fpd, innermost may be less than 50, or less than 40, or less than 30, or less than 20, and in some embodiments, may be less than 10.
- L fpd /D fpd, innermost may be from 0.25-50, or from 0.5 to 40, or from 0.75 to 30, or from 1.0 to 20, or from 1.25 to 10.
- a mixing zone may also be provided in some embodiments, and can be used to mix one or more reactants prior to entry into the expander zone.
- the mixing zone may be fluidly connected to the chamber outlet, or the flow pattern development zone, at the upstream end thereof, and is desirably fluidly connected to the expander zone at its downstream end.
- the mixing zone may be used to bring the reactants, previously introduced into separate inlets, and in some embodiments, passed through the flow pattern development zone, into contact with each other.
- the mixing zone is desirably of a geometry that will allow the flow pattern to be substantially maintained, and in some embodiments, may be cylindrical.
- the mixing zone may advantageously have the same, or a lesser, inner diameter (D m ) as the largest immediately preceding inner diameter, i.e., if fluidly connected to one or more chamber outlets, the mixing zone is desirably substantially the same or smaller, diameter as the outermost chamber outlet. If the mixing zone is fluidly connected to a flow pattern development zone, the mixing zone will desirably be of the same geometry, and have an inner diameter, or cross sectional area, as the case may be, substantially the same as the outermost tube of the flow pattern development zone.
- Any mixing zone may be of any suitable length (L m ), which may be chosen based upon the flow rate and reactivity of the reactants.
- Any mixing zone may have a length, L m , of greater than 1 foot, or greater than 10 feet, or greater than 20 feet, or greater than 30 feet.
- Mixing zone length Lm may be less than 60 feet, or less than 50 feet, or less than 40 feet. In some embodiments, mixing zone length may be from 1 to 60 feet, or from 10 feet to 50 feet, or from 20 feet to 40 feet.
- the ratio of mixing zone length L m to D m may, e.g., be 1, or 2, or 6, or 10. Desirably, the ratio of mixing zone length L m to mixing zone diameter D m will be from 2 to 8.
- the mixer may have an chamber-inlet angle ⁇ of less than 90°, an expander zone having an expander angle ⁇ of ⁇ 45°, and/or i) a chamber inner diameter (D c ) at least 1.25 times greater than the inner diameter of the chamber inlet (D ci ), and/or ii) a chamber inner diameter (D c ) that is at least the same or greater than the inner diameter of the chamber outlet (D co ), and/or iii) a tangential chamber-inlet angle ⁇ of less than 90°, and/or iv) a flow pattern development zone, having a ratio of length (L fpd ) to the inner diameter (D fpd ) of at least 0.5 and/or a mixing zone having a
- Tables 1 and 2 show the possible dimensional relationships that may be optimized in the present mixer and possible values/ranges for each. More particularly, Table 1 contemplates the addition of any number of reactants to the mixer, and Table 2 is directed to those embodiments wherein 2 reactants are introduced via inlets/chambers (although others may be introduced by other means, into other sections of the mixer, e.g., as via injection into a port, etc.)
- Embodiment 1 Embodiment 2 Embodiment 3 Number of 2 or greater 2-10 2-5 inlets/chambers D c (inches) 0.5-120 0.75-90 1.25-60 D c /(D ci ) 1.25-20 1.5-20 2-10 Chamber-inlet angle, ⁇ 90° 5°-85° 10°-80° ⁇ Tangential chamber- 0° or greater 60° to 85° 70° to 80° inlet angle, ⁇ D c /D co 1-10 1.2-8 1.2-4 D fpd, innermost 0.5-60 0.5-30 1-24 L fpd /D fpd, innermost 0.5-30 1-20 1-10 D fpd, outermost NA-60 NA-50 NA-40 L m (feet) 0-60 0-50 0-40 D m (inches) 0.5-120 1.0-60 1.0-36 Expander angle ( ⁇ ) ⁇ 90° 2-45° 3-25° D e (feet) ⁇ 100 ⁇ 50 ⁇ 20
- mixer 100 includes chamber 102 , inlet 104 , and expander 106 , wherein chamber inlet angle, a, is from 10-80°, or 60° and expander angle ⁇ that is desirably >0° but is ⁇ 25°.
- FIG. 1B shows a top view of the mixer shown in FIG. 1A , showing the tangential chamber-inlet angle ⁇ , which is desirably from 10° to 80°.
- chamber outlet 108 is provided by a decrease of 90° in the chamber inner diameter.
- FIG. 1C shows an embodiment wherein the chamber inner diameter is tapered to provide chamber outlet 108 .
- Mixer 100 may accommodate the introduction of one or more reagents/reactants via inlet 104 . Additional reactants/reagents may be introduced at other conventional inlets provided in mixer 100 , such as injection ports (not shown).
- FIG. 2 Another embodiment of the mixer is shown in FIG. 2 .
- Mixer 200 includes two chambers 202 and 203 and inlets 204 and 205 , wherein both chambers are tapered to provide chamber outlets 208 and 209 , respectively.
- FIG. 2B shows a top view of mixer 200 , wherein inlets 204 and 205 are arranged so as to appear superimposed when viewed from the top of mixer 200 .
- FIG. 2C shows an alternative arrangement of inlets 204 and 205 to that shown in FIGS. 2A and 2B .
- Mixer 200 can accommodate the introduction of one or more reactants via inlet 204 , one or more reactants via inlet 205 , and any number of additional reactants introduced by, e.g., injection ports (not shown) as may be provided in mixer 200 .
- FIG. 3 Additional embodiments of the mixer are shown in FIG. 3 .
- the embodiment of mixer 300 shown in FIG. 3A incorporates mixing zone 310 .
- the outlet 308 of chamber 302 and outlet 309 of chamber 303 are arranged concentrically, both ending at the inlet of mixing zone 310 .
- Mixing zone 310 is fluidly connected to expander zone 306 .
- mixer 300 comprises includes flow pattern development zone 312 .
- outlet 308 and outlet 309 are arranged concentrically, with outlet 308 providing the innermost tube of flow pattern development zone 312 .
- Outlet 309 in combination with outlet 308 , provides annular space 313 .
- Outlet 308 , outlet 309 , and annular space 313 each terminate at, and are fluidly connected with, expander zone 306 . In this case, mixing occurs in the expander zone.
- Mixer 300 can accommodate the introduction of one or more reactants via inlet 304 , one or more reactants via inlet 305 , and any number of additional reactants introduced by, e.g., injection ports (not shown) as may be provided in mixer 300 .
- mixer 300 includes both flow pattern development zone and mixing zone 310 .
- the outlets of chambers 302 and 303 are arranged as shown and described in connection with FIG. 3B . And so, in operation of mixer 300 shown in FIG. 3C , one or more reactants may be injected through inlet 304 and one or more reactants may be provided through inlet 305 .
- the desired flow pattern as may be encouraged by the chamber inlet angle ⁇ and tangential chamber-inlet angle ⁇ , may further develop within flow pattern development zone 312 . The reactants would then be mixed within mixing zone 310 .
- FIG. 4A-4C show additional embodiments of the mixer, comprising three inlets.
- mixer 400 includes three inlets and two chambers, with two inlets 405 and 414 being provided to chamber 403 .
- FIG. 4B shows a further embodiment wherein a third chamber 415 is provided, arranged about the same concentric axis as chambers 402 and 403 , but lying within chamber 403 .
- FIG. 4C shows an embodiment of mixer 400 including a third chamber 415 , wherein chamber 415 is arranged about the same concentric axis as chambers 402 and 403 , and between flow pattern development zone 412 and mixing zone 410 .
- third chamber 415 could be provided downstream from, and about the same concentric axis as, chambers 402 and 403 , but upstream from flow pattern development zone 412 .
- Mixer 400 as shown in FIG. 4A-4C include both flow pattern development zone 412 and mixing zone 410 , although this need not be the case, and any of the embodiments of mixer 400 shown in FIG. 4A-4C may be provided only with chambers 402 , 403 and 415 and expander zone 406 .
- the outlet of the mixer may desirably be operably disposed relative to the reactor that would desirably receive the mixed reactants, i.e., the mixer outlet may be directly coupled to a reactor inlet, or may be coupled to any other conduit capable of fluidly coupling the mixer outlet with the reactor inlet.
- Any such conduit is desirably configured so as to be substantially the same shape as the fluid flow from the reactor, e.g., to be substantially tubular or conical. Any such conduit will also desirably be placed about the same longitudinal axis as the outlet of the mixer.
- the advantages provided may be realized or enhanced by using certain reactor features and/or dimensions to assist in the design of the mixer.
- the incorporation of the expander into the present mixer allows an advantageous inlet arrangement to be used, having an inner diameter that more closely approximates the inner diameter of the feedstream source line, while yet having an outlet that more closely approximates the reactor inlet inner diameter.
- Table 2 below, provides a correlation between dimensions and features of the mixer with common reactor sizes with which the mixer may advantageously be used, for an exemplary process wherein two reactants are introduced to two inlet/chambers.
- Table 2 is by no means exhaustive, and those of ordinary skill will be able to extrapolate the dimensions and ranges given to any type of reactor, having any dimensions, and to any type of process.
- the mixer can be attached to a reactor with various configurations.
- a reactor for the production or chlorinated propenes may typically be quite long, and so one or more sections of the reactor and/or mixer may be nonlinear, i.e., one or more zones thereof may comprise bends of 45° or greater, or 90° or greater, or even 135° or greater.
- the reactor and/or mixer may comprise multiple bends, and in such embodiments, may even take the form of a serpentine pattern. Incorporating bends into the reactor and/or mixer allows the desired lengths to be utilized for each zone, while yet minimizing the manufacturing footprint required for the reactor and the mixer.
- the present mixer/reactor apparatus provides significant advantages when used in connection with chemical processes comprising a limiting reagent for which it was designed, and such processes are also provided. Incorporating the present mixer or mixer/reactor apparatus into such a process can reduce, or even eliminate backmixing that may occur in conventional mixers, so that substantial variances in conversions are not seen. Indeed, processes performed using the present mixer and/or apparatus can be provided with minimized production of secondary products and/or decomposition products such that variances of less than 2%, or even less than 1%, from the desired conversion, are seen.
- a reactor provided with such mixer described here may be operated at substantially longer run-time and hence allowed larger capacity than otherwise. Selectivity may also be substantially maintained, or is expected to decrease by no more than 2%.
- Such reactions may also typically include at least one limiting reactant having desired conversions that are far from exhaustion, e.g., conversions of less than 80%, or less than 40%, or even less than 20%.
- the efficiencies provided by the present mixers and apparatus can be further leveraged by providing the chlorinated and/or fluorinated propene and higher alkenes produced therein to further downstream processes.
- 1,1,2,3-tetrachloropropene produced using the described reactors can be processed to provide further downstream products including hydrofluoroolefins, such as, for example, 2,3,3,3-tetrafluoroprop-1-ene (HFO-1234yf) or 1,3,3,3-tetrafluoroprop-1-ene (HFO-1234ze).
- HFO-1234yf 2,3,3,3-tetrafluoroprop-1-ene
- HFO-1234ze 1,3,3,3-tetrafluoroprop-1-ene
- the conversion of chlorinated and/or fluorinated propene and higher alkenes to provide hydrofluoroolefins may broadly comprise a single reaction or two or more reactions involving fluorination of a compound of the formula C(X) m CCl(Y) n (C)(X) m to at least one compound of the formula CF 3 CF ⁇ CHZ, where each X, Y and Z is independently H, F, Cl, I or Br, and each m is independently 1, 2 or 3 and n is 0 or 1.
- a more specific example might involve a multi-step process wherein a feedstock of 1,1,2,3 tetrachloropropene is fluorinated in a catalyzed, gas phase reaction to form a compound such as 2-chloro-3,3,3-tri-fluoropropene.
- the 2-chloro-2,3,3,3-tetrafluoropropane is then dehydrochlorinated to 2,3,3,3-tetrafluoropropene via a catalyzed, gas phase reaction.
- FIGS. 5A and 5B shows two mixers designed to provide a swirling flow pattern to the reactants provided thereto.
- mixer 500 incorporates angle ⁇ of 45°, angle ⁇ of 7°, and angle ⁇ of 60°.
- the flow rate of the reactant provided via inlet 504 is 215.4 kg/hr, while the flow rates of the reactant mixture provided via inlet 505 in the embodiment of mixer 500 shown in FIG. 5A , carbon tetrachloride and perchloroethylene, are 236.5 kg/hr and 10.2 kg/hr, respectively.
- the reactant mixture provided via inlet 505 in FIG. 5A is provided via an injection port (not shown) in FIG.
- the inner diameter of the outermost chamber outlet (D co ), the outermost tube of the flow pattern development zone, and the mixing zone is 1.5′′.
- the flow development zone length (L fpd ) is 8 inches and the mixing zone (L m ) is 12 inches.
- FIGS. 5A and 5B The results of a computational fluid dynamic simulation are also shown in FIGS. 5A and 5B . More specifically, as shown in FIG. 5A , the embodiment of mixer 500 comprising 2 inlets and chambers results in only the formation of a small area of backmixing, indicated by the shaded area within expander zone 506 . Although the backmixing area produced by the embodiment of mixer 500 shown in FIG. 5B is larger, the embodiment of mixer 500 is nonetheless advantageous due to the inclusion of expander zone 506 . That is, mixer 500 shown in FIG. 5B is expected to be much less expensive to manufacture than a mixer not comprising an expander zone, i.e., wherein the mixer outlet closely approximates the inner diameter of a reactor inlet.
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Chemistry (AREA)
- Dispersion Chemistry (AREA)
- Physical Or Chemical Processes And Apparatus (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Accessories For Mixers (AREA)
Abstract
Description
TABLE 1 | |||
Dimension | Embodiment 1 | Embodiment 2 | Embodiment 3 |
Number of | 2 or greater | 2-10 | 2-5 |
inlets/chambers | |||
Dc (inches) | 0.5-120 | 0.75-90 | 1.25-60 |
Dc/(Dci) | 1.25-20 | 1.5-20 | 2-10 |
Chamber-inlet angle, | ≠90° | 5°-85° | 10°-80° |
α | |||
Tangential chamber- | 0° or greater | 60° to 85° | 70° to 80° |
inlet angle, γ | |||
Dc/Dco | 1-10 | 1.2-8 | 1.2-4 |
Dfpd, innermost | 0.5-60 | 0.5-30 | 1-24 |
Lfpd/Dfpd, innermost | 0.5-30 | 1-20 | 1-10 |
Dfpd, outermost | NA-60 | NA-50 | NA-40 |
Lm (feet) | 0-60 | 0-50 | 0-40 |
Dm (inches) | 0.5-120 | 1.0-60 | 1.0-36 |
Expander angle (β) | ≤90° | 2-45° | 3-25° |
De (feet) | ≤100 | ≤50 | ≤20 |
TABLE 2 | ||||
Approximate Reactor ID | 4″ | 8′ | ||
Reactor Dimensions | ||||
ID (Dr), in | 3.826 | 96 | ||
Length, in | 70.87 | 231 | ||
Mixer Dimensions | ||||
Chamber/inlet number | 2 | 2 | ||
Mixer head ID (inch) | 2 | 28 | ||
Inlet 1 ID | (0.1-0.5) | (4-12) | ||
Chamber 1 (central) outlet | ||||
ID | 0.25-0.75 | 4-12 | ||
Inlet 2 ID | 0.1-0.5 | 4-12 | ||
Chamber 2 (outer) outlet | ||||
ID | 0.6-1.4 | 9-27 | ||
Flow pattern development zone, | 3-9 | 12-48 | ||
Length (in) | ||||
Mixing zone, Length (in) | 6-18 | 12-72 | ||
Expander Zone | ||||
Angle from longitudinal axis | 1-20 | 1-20 | ||
Claims (11)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US14/436,604 US10065157B2 (en) | 2012-10-26 | 2013-10-14 | Mixer and processes incorporating the same |
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US201261718920P | 2012-10-26 | 2012-10-26 | |
PCT/US2013/064825 WO2014066083A1 (en) | 2012-10-26 | 2013-10-14 | Mixer and reactor and process incorporating the same |
US14/436,604 US10065157B2 (en) | 2012-10-26 | 2013-10-14 | Mixer and processes incorporating the same |
Publications (2)
Publication Number | Publication Date |
---|---|
US20160158715A1 US20160158715A1 (en) | 2016-06-09 |
US10065157B2 true US10065157B2 (en) | 2018-09-04 |
Family
ID=49514047
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US14/436,604 Expired - Fee Related US10065157B2 (en) | 2012-10-26 | 2013-10-14 | Mixer and processes incorporating the same |
Country Status (7)
Country | Link |
---|---|
US (1) | US10065157B2 (en) |
EP (1) | EP2911773B1 (en) |
JP (1) | JP6363610B2 (en) |
CN (1) | CN104902989B (en) |
CA (1) | CA2887559A1 (en) |
IN (1) | IN2015DN03949A (en) |
WO (1) | WO2014066083A1 (en) |
Families Citing this family (14)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP3366661A1 (en) | 2011-08-07 | 2018-08-29 | Blue Cube IP LLC | Process for the production of chlorinated propenes |
CN103717559A (en) | 2011-08-07 | 2014-04-09 | 陶氏环球技术有限责任公司 | Process for the production of chlorinated propenes |
IN2014CN04029A (en) | 2011-12-02 | 2015-10-23 | Dow Global Technologies Llc | |
EP2785670B1 (en) | 2011-12-02 | 2017-10-25 | Blue Cube IP LLC | Process for the production of chlorinated alkanes |
US9512049B2 (en) | 2011-12-23 | 2016-12-06 | Dow Global Technologies Llc | Process for the production of alkenes and/or aromatic compounds |
US9321707B2 (en) | 2012-09-20 | 2016-04-26 | Blue Cube Ip Llc | Process for the production of chlorinated propenes |
JP2015529247A (en) | 2012-09-20 | 2015-10-05 | ダウ グローバル テクノロジーズ エルエルシー | Process for the production of chlorinated propene |
JP6272878B2 (en) | 2012-09-30 | 2018-01-31 | ブルー キューブ アイピー エルエルシー | Cough quench and method incorporating it |
JP6363610B2 (en) | 2012-10-26 | 2018-07-25 | ブルー キューブ アイピー エルエルシー | Mixer and process incorporating it |
EP2935165A1 (en) | 2012-12-18 | 2015-10-28 | Blue Cube IP LLC | Process for the production of chlorinated propenes |
CN104918904B (en) | 2012-12-19 | 2017-10-31 | 蓝立方知识产权有限责任公司 | Method for producing propylene dichloride |
US9382176B2 (en) | 2013-02-27 | 2016-07-05 | Blue Cube Ip Llc | Process for the production of chlorinated propenes |
WO2014164368A1 (en) | 2013-03-09 | 2014-10-09 | Dow Global Technologies Llc | Process for the production of chlorinated alkanes |
RU185689U1 (en) * | 2018-07-24 | 2018-12-13 | Федеральное государственное бюджетное образовательное учреждение высшего образования "Ивановский государственный политехнический университет" | MEANS FOR MIXING GAS FLOWS |
Citations (234)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US1504443A (en) | 1923-08-25 | 1924-08-12 | James W Gibbons | Paint-spraying apparatus |
GB471187A (en) | 1936-02-28 | 1937-08-30 | Du Pont | Improvements in or relating to the manufacture of chlorinated hydrocarbons |
GB471188A (en) | 1936-02-28 | 1937-08-30 | Du Pont | Improvements in or relating to the manufacture of chlorinated hydrocarbons |
GB471186A (en) | 1936-02-28 | 1937-08-30 | Du Pont | Improvements in or relating to the manufacture of chlorine derivatives of unsaturated hydrocarbons |
US2119484A (en) | 1935-05-06 | 1938-05-31 | Du Pont | Chlorination of propylene dichloride |
US2179378A (en) | 1936-07-18 | 1939-11-07 | Air Reduction | Production of acetylene |
US2207193A (en) | 1937-09-14 | 1940-07-09 | Shell Dev | Production of allyl type halides |
US2299441A (en) | 1939-09-02 | 1942-10-20 | Shell Dev | Catalytic halo-substitution of saturated organic compounds |
US2302228A (en) | 1940-04-02 | 1942-11-17 | Du Pont | Method of chlorination with sulphuryl chloride and production of monochloro-trimethyl acetic acid |
US2370342A (en) | 1940-04-30 | 1945-02-27 | Tide Water Associated Oil Comp | Halogenation |
US2378859A (en) | 1941-08-08 | 1945-06-19 | Distillers Co Yeast Ltd | Splitting-off of hydrogen halide from halogenated hydrocarbons |
US2379551A (en) * | 1944-04-27 | 1945-07-03 | Talley Henry Alfred Ernest | Apparatus for mixing gases |
US2435983A (en) | 1945-12-01 | 1948-02-17 | Universal Oil Prod Co | Production of liquid hydrocarbons |
US2449286A (en) | 1945-07-16 | 1948-09-14 | Shell Dev | Production of 1, 3-dihalopropylenes |
US2588867A (en) | 1948-10-25 | 1952-03-11 | Dow Chemical Co | Pyrolytic production of chlorohydrocarbons |
DE857955C (en) | 1951-03-23 | 1952-12-04 | Basf Ag | Process for the production of tetrachlorethylene in addition to carbon tetrachloride |
US2630461A (en) | 1953-03-03 | Production of acetylene by incom | ||
US2688592A (en) | 1950-10-21 | 1954-09-07 | Diamond Alkali Co | Photochemical process for preparing carbon tetrachloride |
US2762611A (en) | 1952-02-28 | 1956-09-11 | Pfaudler Co Inc | Tubular heat exchangers |
US2765359A (en) | 1953-02-10 | 1956-10-02 | Hydrocarbon Research Inc | Production of acetylene |
US2964579A (en) | 1958-10-09 | 1960-12-13 | Houdry Process Corp | Selective hydrogenation of diolefins with copper chromite catalyst |
GB857086A (en) | 1956-08-30 | 1960-12-29 | Hoechst Ag | Process for the manufacture of carbon tetrachloride |
US2973393A (en) | 1958-10-02 | 1961-02-28 | Dow Chemical Co | Chlorination of acetylenes |
US3000980A (en) | 1958-04-07 | 1961-09-19 | Dow Chemical Co | Preparation of alkyl bromides |
US3094567A (en) | 1960-02-25 | 1963-06-18 | Monsanto Chemicals | Chlorination of propynes |
US3112988A (en) | 1960-02-26 | 1963-12-03 | Sheil Oil Company | Mixing gases at supersonic velocity |
LU52247A1 (en) | 1966-06-07 | 1966-12-28 | ||
FR1546709A (en) | 1967-10-10 | 1968-11-22 | Mini Ind Chimice | Method and apparatus for the continuous system manufacture of hydrocarbon nitroso-derivatives |
GB1134585A (en) | 1966-07-22 | 1968-11-27 | Knapsack Ag | Process for the joint manufacture of 2,2,3-trichlorobutane and 1,2,3-trichlorobutane |
US3444263A (en) | 1966-11-09 | 1969-05-13 | Gulf Research Development Co | Method for converting ethylene to alpha olefins in the presence of an organic sulfide |
US3446859A (en) | 1962-06-11 | 1969-05-27 | Hooker Chemical Corp | Vapor phase condensation process |
US3502734A (en) | 1966-05-11 | 1970-03-24 | Du Pont | Process for partially chlorinating methyl chloride and/or methylene chloride |
US3525595A (en) | 1967-05-19 | 1970-08-25 | Bayer Ag | Concentric cross flow nozzle apparatus for carrying out reactions between gases |
US3551512A (en) | 1968-11-01 | 1970-12-29 | Diamond Shamrock Corp | Pressure process for preparing acetylene |
US3558438A (en) | 1968-10-30 | 1971-01-26 | Du Pont | Distillation process and apparatus |
US3615202A (en) * | 1969-11-28 | 1971-10-26 | David R Stern | Process for the manufacture of titanium dioxide |
US3651019A (en) | 1961-09-28 | 1972-03-21 | Yeda Res & Dev | Production of adducts of carbon tetrachloride or chloroform with olefinically unsaturated substances |
US3676508A (en) | 1969-01-30 | 1972-07-11 | Hornig Anneliese | Process for the manufacture of carbon tetrachloride |
US3819731A (en) | 1960-03-23 | 1974-06-25 | Stauffer Chemical Co | Production of chlorinated unsaturated hydrocarbons |
US3823195A (en) | 1971-12-27 | 1974-07-09 | Monsanto Co | Preparation of 1,1,2,3-tetrachloropropene from 1,2,3-trichloropropane |
GB1381619A (en) | 1971-12-17 | 1975-01-22 | Monsanto Co | Process for the production of 1,2,3-trichloropropene |
US3872664A (en) | 1973-10-15 | 1975-03-25 | United Aircraft Corp | Swirl combustor with vortex burning and mixing |
US3914167A (en) | 1974-08-26 | 1975-10-21 | Dow Chemical Co | Process for making cis-1,3-dichloropropene |
US3920757A (en) | 1971-08-25 | 1975-11-18 | Dow Chemical Co | Chlorination with sulfuryl chloride |
US3926758A (en) | 1971-12-27 | 1975-12-16 | Monsanto Co | Preparation of 1,1,2,3-tetrachloropropene from 2,3-trichloropropane |
US3948858A (en) | 1973-09-22 | 1976-04-06 | Akzo N.V. | Polymerization of ethylenically unsaturated compounds |
US3954410A (en) | 1972-11-21 | 1976-05-04 | Merck Patent Gesellschaft Mit Beschraenkter Haftung | Solvents for NMR spectroscopy |
US4038372A (en) | 1976-05-05 | 1977-07-26 | The United States Of America As Represented By The Secretary Of The Navy | Process for manufacturing chloramine |
US4043766A (en) * | 1975-11-20 | 1977-08-23 | Dr. C. Otto & Comp. G.M.B.H. | Slag bath generator |
US4046656A (en) | 1976-12-06 | 1977-09-06 | The Dow Chemical Company | Photochlorination process for methyl aromatic compounds |
US4051182A (en) | 1976-04-12 | 1977-09-27 | Stauffer Chemical Company | Process for the manufacture of α-chloropropionyl chloride |
JPS544869A (en) | 1977-06-15 | 1979-01-13 | Babcock Hitachi Kk | Mixer for reducing agent and diluting agent |
CH609022A5 (en) | 1973-06-12 | 1979-02-15 | Monsanto Co | Process for the preparation of 1,2,3-trichloropropene from 1,2,3-trichloropropane |
US4145187A (en) * | 1974-03-21 | 1979-03-20 | Matthey Rustenburg Refiners (Pty.) Ltd. | Treatment of material with hydrogen chloride |
JPS5479207A (en) | 1977-12-05 | 1979-06-25 | Showa Denko Kk | Preparation of 1,3-dichloropropene |
GB1548277A (en) | 1971-07-30 | 1979-07-11 | Allied Chem | Process for chlorination of hydrocarbons |
JPS54135712A (en) | 1978-04-13 | 1979-10-22 | Osaka Soda Co Ltd | Prepartion of 3-chloropropene |
SU899523A1 (en) | 1979-07-03 | 1982-01-23 | Уфимский Нефтяной Институт | Process for producing 1,1,2,3-tetrachloropropene |
US4319062A (en) | 1976-08-02 | 1982-03-09 | The Dow Chemical Company | Allyl chloride process |
WO1982001728A1 (en) | 1980-11-17 | 1982-05-27 | Manders Petrus G | A method for conveying a flexible thread by means of a pressurized gas |
US4381187A (en) * | 1980-03-24 | 1983-04-26 | United Technologies Corporation | Process for gasifying liquid hydrocarbon fuels |
DD209184A1 (en) | 1982-07-02 | 1984-04-25 | Buna Chem Werke Veb | PROCESS FOR THE PREPARATION OF CHLOROPROPENES |
US4513154A (en) | 1971-07-30 | 1985-04-23 | Allied Corporation | Process for consecutive competitive gas phase reaction |
US4535194A (en) | 1983-07-06 | 1985-08-13 | Monsanto Co. | Process for producing 1,1,2,3-tetrachloropropene |
EP0164798A1 (en) | 1981-09-01 | 1985-12-18 | George Andrew Olah | Process for the preparation of methyl monohalides |
DD235631A1 (en) | 1985-03-25 | 1986-05-14 | Buna Chem Werke Veb | PROCESS FOR THE PREPARATION OF CHLOROPROPENES FROM 1,2-DICHLORPROPANE |
US4614572A (en) | 1985-07-08 | 1986-09-30 | The Dow Chemical Company | Liquid phase chlorination of chlorinated methanes |
US4644907A (en) | 1985-11-29 | 1987-02-24 | Hunter Edward H | Boiler tubes of enhanced efficiency and method of producing same |
US4650914A (en) | 1983-07-06 | 1987-03-17 | Monsanto Company | Process for producing 1,1,2,3-tetrachloropropene |
US4661648A (en) | 1984-08-20 | 1987-04-28 | Solvay & Cie (Societe Anonyme) | Process for carrying out substitution chlorination reactions of organic compounds by means of molecular chlorine in the presence of a chlorinated product serving as a radical initiator, and radical initiators used in such a process |
US4702809A (en) | 1984-04-25 | 1987-10-27 | Huels Aktiengesellschaft | Process for the production of 1,2,3-trichloro-2-methylpropane |
US4714792A (en) | 1984-09-06 | 1987-12-22 | Huels Aktiengesellschaft | Process for the production of 1,2,3-trichloropropane |
US4716255A (en) | 1983-08-25 | 1987-12-29 | Huels Aktiengesellschaft | Process for the production of 3,3-dichloro-2-methylpropene |
US4727181A (en) | 1986-04-21 | 1988-02-23 | The Dow Chemical Company | Process for the preparation of α-halocinnamate esters |
US4726686A (en) | 1985-07-30 | 1988-02-23 | Hartmut Wolf | Swirl chamber |
US4849554A (en) | 1987-04-10 | 1989-07-18 | Imperial Chemical Industries Plc | Production of tetrafluoroethylene and hexafluoropropylene |
US4894205A (en) | 1987-09-18 | 1990-01-16 | Shell Oil Company | Multitube reactor |
US4902393A (en) | 1983-08-25 | 1990-02-20 | Huels Aktiengesellschaft | Process for the production of 1,1,2-trichloro-2-methylpropane |
US4999102A (en) | 1988-12-16 | 1991-03-12 | The Amalgamated Sugar Company | Liquid transfer manifold system for maintaining plug flow |
US5057634A (en) | 1989-12-19 | 1991-10-15 | E. I. Du Pont De Nemours And Company | Multistep synthesis of hexafluoropropylene |
EP0453818A1 (en) | 1990-04-13 | 1991-10-30 | Ec Erdölchemie Gmbh | Process for the reductive dehalogenation of halogenated hydrocarbons and halogenated ethers |
US5132473A (en) | 1988-05-17 | 1992-07-21 | Daikin Industries, Ltd. | Process for production of 1,1,1-trifluoro-2,2-dichloroethane |
US5171899A (en) | 1988-05-17 | 1992-12-15 | Daikin Industries Ltd. | Process for production of 1,1,1-trifluoro-2,2-dichloroethane |
US5178844A (en) | 1990-04-03 | 1993-01-12 | Phillips Petroleum Company | Method and apparatus for producing nitride products |
US5246903A (en) | 1987-05-26 | 1993-09-21 | The Dow Chemical Company | Process and catalyst for the dehydrohalogenation of halogenated hydrocarbons or alkylene halohydrins |
US5254772A (en) | 1991-03-12 | 1993-10-19 | Imperial Chemical Industries Plc | Chemical process |
US5254771A (en) | 1989-07-14 | 1993-10-19 | Hoechst Aktiengesellschaft | Process for the preparation of 1,1,1-trifluoro-2-2-dichloroethane under elevated pressure |
US5254788A (en) | 1991-09-10 | 1993-10-19 | Stone And Webster Engineering Corporation | Process for the production of olefins from light paraffins |
US5262575A (en) | 1992-08-04 | 1993-11-16 | The Dow Chemical Company | Production of allylic chlorides |
US5367105A (en) | 1992-10-23 | 1994-11-22 | Tokuyama Corporation | Process and device for production of allyl chloride |
US5414166A (en) | 1993-11-29 | 1995-05-09 | Korea Institute Of Science And Technology | Process for the preparation of 1,1,1-trifluoro-2,2-dichloroethane |
US5504266A (en) | 1995-05-24 | 1996-04-02 | The Dow Chemical Company | Process to make allyl chloride and reactor useful in that process |
JPH08119885A (en) | 1994-10-25 | 1996-05-14 | Central Glass Co Ltd | Production of fluorinated hydrocarbon |
US5684219A (en) | 1995-08-28 | 1997-11-04 | Laroche Industries Inc. | Process for preparing fluorinated aliphatic compounds |
US5689020A (en) | 1996-03-11 | 1997-11-18 | Laroche Industries Inc. | High temperature chlorination process for the preparation of polychloroolefins |
US5811605A (en) | 1997-02-19 | 1998-09-22 | Ppg Industries, Inc. | Preparation of 1,2,3,3-tetrachloropropene |
WO1999006314A1 (en) | 1997-07-31 | 1999-02-11 | E.I. Du Pont De Nemours And Company | Air jet piddling |
US5895825A (en) | 1997-12-01 | 1999-04-20 | Elf Atochem North America, Inc. | Preparation of 1,1,1,3,3-pentafluoropropane |
US5986151A (en) | 1997-02-05 | 1999-11-16 | Alliedsignal Inc. | Fluorinated propenes from pentafluoropropane |
US6111150A (en) | 1996-06-20 | 2000-08-29 | Central Glass Company, Limited | Method for producing 1,1,1,3,3,-pentafluoropropane |
US6118018A (en) | 1999-12-06 | 2000-09-12 | Occidental Chemical Corporation | Chlorination and bromination of aromatic compounds at atmospheric pressure |
US6160187A (en) | 1997-12-18 | 2000-12-12 | The Dow Chemical Company | Method for making glycol in an adiabatic reactor system |
US6187976B1 (en) | 1998-04-09 | 2001-02-13 | Alliedsignal Inc. | Process for the preparation of fluorine containing hydrohalocarbons |
US6229057B1 (en) | 1993-07-26 | 2001-05-08 | Zeneca Limited | Chlorination process |
EP1097984A2 (en) | 1999-11-02 | 2001-05-09 | Noell-KRC Energie- und Umwelttechnik GmbH | Process and plant for the cooling and cleaning of gasification gases |
US6235951B1 (en) | 1996-01-17 | 2001-05-22 | Central Glass Company, Limited | Method for producing 1,1,1,3,3-pentafluoropropane |
WO2001038275A1 (en) | 1999-11-22 | 2001-05-31 | The Dow Chemical Company | Dehydrohalogenation of halogenated alkanes using rare earth halide or oxyhalide catalyst |
JP2001151708A (en) | 1999-11-22 | 2001-06-05 | Central Glass Co Ltd | Method for producing 1,1,1,3,3-pentachloropropane |
JP2001213820A (en) | 2000-01-31 | 2001-08-07 | Central Glass Co Ltd | Method of producing 1,1,1,3,3-pentachloro-propane |
US20010018962A1 (en) | 1998-12-23 | 2001-09-06 | American Air Liquide Inc. | Heat exchanger for preheating an oxidizing gas |
US20020087039A1 (en) | 2000-12-29 | 2002-07-04 | Tung Hsueh Sung | Method of making hydrofluorocarbons and hydrochlorofluorocarbons |
US20020110711A1 (en) | 2000-11-04 | 2002-08-15 | Stefan Boneberg | Method and device for starting a reacator in a gas-generating system |
US6472573B1 (en) | 1998-03-23 | 2002-10-29 | Daikin Industries, Ltd. | Process for producing 1,1,1,3,3-pentafluoropropane |
US6538167B1 (en) | 1996-10-02 | 2003-03-25 | Exxonmobil Chemical Patents Inc. | Process for producing light olefins |
US6545176B1 (en) | 1998-11-04 | 2003-04-08 | Rohm And Haas Company | Apparatus and process for the high yield production of methyl methacrylate or methacrylic acid |
US6551469B1 (en) | 2001-11-27 | 2003-04-22 | Honeywell International | Photochlorination of 1,1,1,3,3-pentafluoropropane |
US6613127B1 (en) | 2000-05-05 | 2003-09-02 | Dow Global Technologies Inc. | Quench apparatus and method for the reformation of organic materials |
US6683216B1 (en) | 2002-11-06 | 2004-01-27 | Eastman Chemical Company | Continuous process for the preparation of amines |
US6825383B1 (en) | 2003-09-22 | 2004-11-30 | Council Of Scientific And Industrial Research | Catalytic process for regiospecific chlorination of alkanes, alkenes and arenes |
WO2005016509A1 (en) | 2003-07-31 | 2005-02-24 | Dow Global Technologies Inc. | Oxidation process and reactor with modified feed system |
US6924403B2 (en) | 2002-06-26 | 2005-08-02 | E. I. Du Pont De Nemours And Company | Synthesis of hexafluoropropylene |
US6958135B1 (en) | 1999-06-15 | 2005-10-25 | Methanol Casale S.A. | Isothermal reactor for exothermic or endothermic heterogeneous reactions |
US20060150445A1 (en) | 2003-01-24 | 2006-07-13 | Redding John H | Underwater sediment management |
US7117934B2 (en) | 2002-03-15 | 2006-10-10 | H2Gen Innovations, Inc. | Method and apparatus for minimizing adverse effects of thermal expansion in a heat exchange reactor |
JP2006272267A (en) | 2005-03-30 | 2006-10-12 | Fuji Photo Film Co Ltd | Method of operating microchemical device |
US7140558B2 (en) * | 2003-03-24 | 2006-11-28 | Irene Base, legal representative | Mixing arrangement for atomizing nozzle in multi-phase flow |
US20060292046A1 (en) | 2003-07-31 | 2006-12-28 | Dow Global Technologies Inc. | Oxidation process and reactor with modified feed system |
JP2007021396A (en) | 2005-07-19 | 2007-02-01 | Japan Science & Technology Agency | Method for removing heavy metal |
US7172733B2 (en) * | 2002-05-06 | 2007-02-06 | Institut Francais Du Petrole | Device for injection of hydrocarbons into a fluidized chamber |
US7189884B2 (en) | 2004-04-29 | 2007-03-13 | Honeywell International | Processes for synthesis of tetrafluoropropene |
DE102005044501A1 (en) | 2005-09-16 | 2007-03-22 | Roquette, Eberhard, Dipl.-Ing. | Preparation of ester containing alcohol and fatty acid by nozzle system (venturi principle) comprising nozzle fitter or holder, mixing tube, diffuser and two chamber mixing system |
US7226567B1 (en) | 1999-03-16 | 2007-06-05 | Basf Aktiengesellschaft | Multi-tube fixed-bed reactor, especially for catalytic gas phase reactions |
WO2007079435A2 (en) | 2006-01-03 | 2007-07-12 | Honeywell International Inc. | Method for producing fluorinated organic compounds |
WO2007079431A2 (en) | 2006-01-03 | 2007-07-12 | Honeywell International Inc. | Method for producing fluorinated organic compounds |
US20070197841A1 (en) | 2004-04-29 | 2007-08-23 | Honeywell International Inc. | Method for producing fluorinated organic compounds |
US20070197842A1 (en) | 2004-04-29 | 2007-08-23 | Honeywell International Inc. | Method for producing fluorinated organic compounds |
WO2007096383A1 (en) | 2006-02-21 | 2007-08-30 | Sachtleben Chemie Gmbh | Method for carrying out chemical and physical processes and reaction cells |
US7282120B2 (en) | 1999-06-16 | 2007-10-16 | Solvay Fluor Gmbh | UV-activated chlorination process |
US20070259296A1 (en) * | 2004-12-23 | 2007-11-08 | Knoepfel Hans P | Premix Burner With Mixing Section |
US20070265368A1 (en) | 2004-12-22 | 2007-11-15 | Velliyur Nott Mallikarjuna Rao | Functionalized Copolymers of Terminally Functionalized Perfluoro (Alkyl Vinyl Ether) Reactor Wall for Photochemical Reactions, Process for Increasing Fluorine Content in Hydrocaebons and Halohydrocarbons and Olefin Production |
US7297814B2 (en) | 2002-01-11 | 2007-11-20 | Mitsubishi Chemical Corporation | Multitube reactor, vapor phase catalytic oxidation method using the multitube reactor, and start up method applied to the multitube reactor |
US20080021229A1 (en) | 2004-05-21 | 2008-01-24 | Maughon Bob R | Process for Preparing Epichlorhydrin from Ethane |
US7345209B2 (en) | 2004-04-29 | 2008-03-18 | Honeywell International Inc. | Processes for synthesis of 1,3,3,3-tetrafluoropropene |
JP2008063314A (en) | 2006-09-04 | 2008-03-21 | Tokyo Kasei Kogyo Kk | Environment-conscious hypervalent iodine reagent |
US20080073063A1 (en) | 2006-06-23 | 2008-03-27 | Exxonmobil Research And Engineering Company | Reduction of fouling in heat exchangers |
WO2008054781A1 (en) | 2006-10-31 | 2008-05-08 | E. I. Du Pont De Nemours And Company | Processes for the production of fluoropropanes and halopropenes and azeotropic compositions of 2-chloro-3,3,3-trifluoro-1-propene with hf and of 1,1,1,2,2-pentafluoropropane with hf |
US7371904B2 (en) | 2004-04-29 | 2008-05-13 | Honeywell International Inc. | Processes for synthesis of 1,3,3,3-tetrafluoropropene |
US20080118018A1 (en) | 2004-12-10 | 2008-05-22 | Schrauwen Franciscus Johannes | Reactor Tube Apparatus |
US7378559B2 (en) | 2003-03-07 | 2008-05-27 | Dow Global Technologies Inc. | Continuous process and system of producing polyether polyols |
US7396965B2 (en) | 2005-05-12 | 2008-07-08 | Honeywell International Inc. | Method for producing fluorinated organic compounds |
CN101215220A (en) | 2008-01-16 | 2008-07-09 | 西安近代化学研究所 | Preparation method for 1,1,1,3-tetrafluoropropene |
US20080207962A1 (en) | 2007-02-23 | 2008-08-28 | Velliyur Nott Mallikarjuna Rao | Compositions containing chromium, oxygen, and at least two modifier metals selected the group consisting of gold, silver, and palladium, their preparation, and their use as catalysts and catalyst precursors |
JP2009000592A (en) | 2007-06-19 | 2009-01-08 | Hitachi Ltd | Reactor and reaction system |
US20090018377A1 (en) | 2007-07-09 | 2009-01-15 | Boyce C Bradford | Catalytic process for the preparation of fluorinated halocarbons |
US20090030249A1 (en) | 2007-07-25 | 2009-01-29 | Honeywell International Inc. | Processes for preparing 1,1,2,3-tetrachloropropene |
JP2009046653A (en) | 2007-07-24 | 2009-03-05 | Nagase Chemtex Corp | Method for producing polymer of aromatic compound and heterocyclic aromatic compound by using hypervalent iodine reagent |
US7511101B2 (en) | 2005-05-13 | 2009-03-31 | Fina Technology, Inc. | Plug flow reactor and polymers prepared therewith |
US20090088547A1 (en) | 2006-10-17 | 2009-04-02 | Rpo Pty Limited | Process for producing polysiloxanes and use of the same |
US20090099396A1 (en) | 2007-10-15 | 2009-04-16 | Honeywell International Inc. | Process for synthesis of fluorinated olefins |
US7521029B2 (en) | 2003-01-31 | 2009-04-21 | Man Dwe Gmbh | Shell-and-tube type reactor for carrying out catalytic gaseous phase reactions and a procedure for operating the same |
US20090117014A1 (en) | 2007-11-06 | 2009-05-07 | Quantumsphere, Inc. | System and method for ammonia synthesis |
WO2009067571A1 (en) | 2007-11-20 | 2009-05-28 | E. I. Du Pont De Nemours And Company | Synthesis of hydrofluoroalkanols and hydrofluoroalkenes |
WO2009087423A1 (en) | 2008-01-11 | 2009-07-16 | John Redding | Improvements in or relating to jet nozzles |
CN101492341A (en) | 2009-03-05 | 2009-07-29 | 杨海珍 | Process for producing saturated polychloralkane |
US20090203945A1 (en) | 2007-08-22 | 2009-08-13 | Honeywell International Inc. | Method for producing fluorinated organic compounds |
US7588739B2 (en) | 2003-07-14 | 2009-09-15 | Mitsubishi Rayon Co., Ltd. | Fixed bed multitube reactor |
CN101544535A (en) | 2009-05-01 | 2009-09-30 | 浙江三美化工股份有限公司 | Method for preparing synthetic 1,1,1,3,3-pentachloro propane |
US20090270568A1 (en) | 2006-06-26 | 2009-10-29 | Solvay (Société Anonyme) | Process for the Manufacture of 1,2-Dichloroethane |
CN101597209A (en) | 2008-03-20 | 2009-12-09 | 霍尼韦尔国际公司 | Be used to prepare 2,3,3, the integrated process of 3-tetrafluoeopropene |
US7659434B2 (en) | 2004-04-29 | 2010-02-09 | Honeywell International Inc. | Method for producing fluorinated organic compounds |
US20100041864A1 (en) | 2007-04-10 | 2010-02-18 | Asahi Glass Company, Limited | Double metal cyanide complex catalyst having organic ligand, process for its production and method for producing polyether polyol |
US7674939B2 (en) | 2004-04-29 | 2010-03-09 | Honeywell International Inc. | Method for producing fluorinated organic compounds |
US7687670B2 (en) | 2006-03-31 | 2010-03-30 | E.I. Du Pont De Nemours And Company | Coproduction of hydrofluoroolefins |
US7695695B2 (en) | 2006-01-18 | 2010-04-13 | Lg Chem, Ltd. | Reactor or heat exchanger with improved heat transfer performance |
US20100185029A1 (en) | 2007-06-27 | 2010-07-22 | Arkema Inc. | Two step process for the manufacture of hydrofluoroolefins |
US20100263278A1 (en) | 2007-09-18 | 2010-10-21 | Uhde Gmbh | Gasification reactor and process for entrained-flow gasification |
US7836941B2 (en) | 2006-05-19 | 2010-11-23 | Exxonmobil Research And Engineering Company | Mitigation of in-tube fouling in heat exchangers using controlled mechanical vibration |
CN101913979A (en) | 2010-09-07 | 2010-12-15 | 西安近代化学研究所 | Production method of 1,1,1,3,3-pentachlorobutane |
CN101913980A (en) | 2010-09-07 | 2010-12-15 | 西安近代化学研究所 | Production method of 1,1,1,3,3-pentachloropropane |
CN101955414A (en) | 2010-04-20 | 2011-01-26 | 南通泰禾化工有限公司 | Technology for preparing 1, 1, 2, 3-tetrachloropropene |
US7880040B2 (en) | 2004-04-29 | 2011-02-01 | Honeywell International Inc. | Method for producing fluorinated organic compounds |
CN101982227A (en) | 2010-09-15 | 2011-03-02 | 山东东岳高分子材料有限公司 | Rapid gas hybrid reactor for high temperature cracking and application thereof |
CN102001911A (en) | 2010-09-20 | 2011-04-06 | 西安近代化学研究所 | Method for preparing 2,3,3,3-tetrafluoropropene |
US20110087056A1 (en) | 2009-10-09 | 2011-04-14 | Dow Global Technologies | Adiabatic plug flow reactors and processes incorporating the same |
WO2011060211A1 (en) | 2009-11-16 | 2011-05-19 | Arkema Inc. | Method to purify and stabilize chloroolefins |
US7951982B2 (en) | 2004-04-29 | 2011-05-31 | Honeywell International Inc. | Method for producing fluorinated organic compounds |
WO2011065574A1 (en) | 2009-11-27 | 2011-06-03 | Daikin Industries, Ltd. | Process for preparing 1,1,2,3-tetrachloropropene |
US20110155942A1 (en) | 2009-12-23 | 2011-06-30 | Arkema France | Catalytic Gas Phase Fluorination of 1230xa to 1234yf |
US20110172472A1 (en) | 2008-09-25 | 2011-07-14 | Central Glass Company, Limited | Process for Producing 1,3,3,3-Tetrafluoropropene |
JP2011144148A (en) | 2010-01-18 | 2011-07-28 | Nippon Zeon Co Ltd | Hydrogen-containing halogenated cyclopentane, and method for producing heptafluorocyclopentene |
US20110218369A1 (en) | 2008-11-19 | 2011-09-08 | Arkema Inc. | Process for the manufacture of hydrofluoroolefins |
US20110251425A1 (en) | 2008-08-07 | 2011-10-13 | Basf Se | Process for preparing aromatic isocyanates |
US8058486B2 (en) | 2004-04-29 | 2011-11-15 | Honeywell International Inc. | Integrated process to produce 2,3,3,3-tetrafluoropropene |
CN102249846A (en) | 2011-05-31 | 2011-11-23 | 浙江师范大学 | Co-production preparation method of 2-chloro-3,3,3-trifluoropropene and 2,3-dichloro-1,1-difluoro propylene |
DE102010022414A1 (en) | 2010-06-01 | 2011-12-01 | Günther Kramb jun. | Emulsifying device for emulsifying two or multiple substances used in beverage industry, chemical industry, pharmaceutical industry and medicines, has housing which encloses reaction chamber that has inlets for both mediums |
US8071825B2 (en) | 2006-01-03 | 2011-12-06 | Honeywell International Inc. | Method for producing fluorinated organic compounds |
US8071826B2 (en) | 2008-04-04 | 2011-12-06 | Honeywell International Inc. | Process for the preparation of 2,3,3,3-tetrafluoropropene (HFO-1234yf) |
US8076521B2 (en) | 2007-06-27 | 2011-12-13 | Arkema Inc. | Process for the manufacture of hydrofluoroolefins |
WO2012011844A1 (en) | 2010-07-21 | 2012-01-26 | Открытое Акционерное Общество "Научно-Исследовательский И Проектный Институт Карбамида И Продуктов Органического Синтеза" (Оао Ниик) | Gas-liquid reactor (variant embodiments) |
US8115038B2 (en) | 2007-12-19 | 2012-02-14 | Occidental Chemical Corporation | Methods of making chlorinated hydrocarbons |
CN102351637A (en) | 2011-08-31 | 2012-02-15 | 浙江师范大学 | Method for preparing 2,3,3,3-tetrafluoropropene |
US8123398B2 (en) | 2005-08-09 | 2012-02-28 | Canon Kabushiki Kaisha | Fluid-processing device |
US20120065434A1 (en) | 2009-05-13 | 2012-03-15 | Masatoshi Nose | Process for preparing chlorine-containing fluorocarbon compound |
WO2012081482A1 (en) | 2010-12-16 | 2012-06-21 | 株式会社トクヤマ | Method for producing c3 chlorinated hydrocarbon |
US8232435B2 (en) | 2006-09-05 | 2012-07-31 | E I Du Pont De Nemours And Company | 1,2,3,3,3-pentafluoropropene production processes |
US8258353B2 (en) | 2008-10-13 | 2012-09-04 | Dow Global Technologies, Llc | Process for the production of chlorinated and/or fluorinated propenes |
WO2012166393A1 (en) | 2011-05-31 | 2012-12-06 | Dow Global Technologies, Llc | Process for the production of chlorinated propenes |
WO2012166394A1 (en) | 2011-05-31 | 2012-12-06 | Dow Global Technologies, Llc | Process for the production of chlorinated propenes |
US8357828B2 (en) | 2008-12-25 | 2013-01-22 | Asahi Glass Company, Limited | Processes for producing 1,1-dichloro-2,3,3,3-tetrafluoropropene and 2,3,3,3-tetrafluoropropene |
US8367867B2 (en) | 2007-10-04 | 2013-02-05 | Urea Casale S.A. | Process and plant for urea production |
US8383867B2 (en) | 2004-04-29 | 2013-02-26 | Honeywell International Inc. | Method for producing fluorinated organic compounds |
WO2013082410A1 (en) | 2011-12-02 | 2013-06-06 | Dow Global Technologies, Llc | Process for the production of chlorinated alkanes |
US8558041B2 (en) | 2009-10-09 | 2013-10-15 | Dow Global Technologies, Llc | Isothermal multitube reactors and processes incorporating the same |
US8581012B2 (en) | 2009-10-09 | 2013-11-12 | Dow Global Technologies, Llc | Processes for the production of chlorinated and/or fluorinated propenes and higher alkenes |
US8581011B2 (en) | 2009-10-09 | 2013-11-12 | Dow Global Technologies, Llc | Process for the production of chlorinated and/or fluorinated propenes |
US8614361B2 (en) | 2009-04-23 | 2013-12-24 | Daikin Industries, Ltd. | Process for preparation of 2,3,3,3-tetrafluoropropene |
WO2014046970A1 (en) | 2012-09-20 | 2014-03-27 | Dow Global Technologies, Llc | Process for the production of chlorinated propenes |
WO2014046977A1 (en) | 2012-09-20 | 2014-03-27 | Dow Global Technologies, Llc | Process for the production of chlorinated propenes |
WO2014066083A1 (en) | 2012-10-26 | 2014-05-01 | Dow Global Technologies, Llc | Mixer and reactor and process incorporating the same |
US20140163266A1 (en) | 2011-08-07 | 2014-06-12 | Dow Global Technologies Llc | Process for the production of chlorinated propenes |
US20140179962A1 (en) | 2011-08-07 | 2014-06-26 | Dow Global Technologies Llc | Process for the production of chlorinated propenes |
WO2014100039A1 (en) | 2012-12-19 | 2014-06-26 | Dow Global Technologies, Llc | Process for the production of chlorinated propenes |
WO2014100066A1 (en) | 2012-12-18 | 2014-06-26 | Dow Global Technologies, Llc | Process for the production of chlorinated propenes |
WO2014134233A2 (en) | 2013-02-27 | 2014-09-04 | Dow Global Technologies Llc | Process for the production of chlorinated propenes |
WO2014134377A2 (en) | 2013-02-28 | 2014-09-04 | Dow Global Technologies Llc | Process for the production of chlorinated propanes |
WO2014164368A1 (en) | 2013-03-09 | 2014-10-09 | Dow Global Technologies Llc | Process for the production of chlorinated alkanes |
US20140323775A1 (en) | 2011-12-02 | 2014-10-30 | Dow Global Technologies Llc | Process for the production of chlorinated alkanes |
US20140336431A1 (en) | 2011-12-23 | 2014-11-13 | Dow Global Technologies Llc | Process for the production of alkenes and/or aromatic compounds |
US20140336425A1 (en) | 2011-12-22 | 2014-11-13 | Dow Global Technologies Llc | Process for the production of tetrachloromethane |
US20140371494A1 (en) | 2011-12-13 | 2014-12-18 | Dow Global Technologies Llc | Process for the production of chlorinated propanes and propenes |
US20150045592A1 (en) | 2011-11-21 | 2015-02-12 | Dow Global Technologies Llc | Process for the production of chlorinated alkanes |
US8957258B2 (en) | 2012-01-24 | 2015-02-17 | Kanto Denka Kogyo Co., Ltd. | BIS(1,1-Dichloro-3,3,3-trifluoropropyl) ether and process for preparing the same |
US20150057471A1 (en) | 2011-12-23 | 2015-02-26 | Dow Global Technologies Llc | Chlorinating agents |
US20150217256A1 (en) | 2012-09-30 | 2015-08-06 | Dow Global Technologies Llc | Weir quench and processes incorporating the same |
Family Cites Families (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS4837648Y1 (en) * | 1967-03-04 | 1973-11-08 | ||
ATE723T1 (en) * | 1978-09-20 | 1982-03-15 | Jacques G. Kempf | PROCESS AND EQUIPMENT FOR ENERGY RECOVERY IN THE PRODUCTION OF POLYMER FROM MONOMER GAS. |
DE3115391A1 (en) * | 1981-04-16 | 1982-12-30 | Bergwerksverband Gmbh, 4300 Essen | "METHOD AND DEVICE FOR THE PRODUCTION OF HYDROGEN AND CARBON OXIDE GASES FROM RAW CARBON DISTILLATION GASES |
SU1042784A1 (en) * | 1981-07-31 | 1983-09-23 | Уральский Филиал Всесоюзного Научно-Исследовательского И Проектного Института Алюминиевой,Магниевой И Электродной Промышленности | Spray apparatus |
CN2202583Y (en) * | 1994-09-21 | 1995-07-05 | 中国科学院声学研究所 | Sound resonant cavity jet current emulsator |
GB0113735D0 (en) * | 2001-06-05 | 2001-07-25 | Holset Engineering Co | Mixing fluid streams |
DE10133729A1 (en) * | 2001-07-11 | 2003-01-23 | Bayer Ag | Process for the preparation of (cyclo) aliphatic diisocyanates |
CN102317254B (en) * | 2008-07-23 | 2014-11-19 | 巴斯夫欧洲公司 | Method for producing isocyanates |
CN101708438B (en) * | 2009-12-04 | 2011-12-28 | 天津大学 | Mixer and method for preparing organic isocyanate |
CN201921642U (en) * | 2010-12-04 | 2011-08-10 | 金川集团有限公司 | Gas-liquid mixing device |
-
2013
- 2013-10-14 JP JP2015539650A patent/JP6363610B2/en not_active Expired - Fee Related
- 2013-10-14 IN IN3949DEN2015 patent/IN2015DN03949A/en unknown
- 2013-10-14 WO PCT/US2013/064825 patent/WO2014066083A1/en active Application Filing
- 2013-10-14 CA CA2887559A patent/CA2887559A1/en not_active Abandoned
- 2013-10-14 CN CN201380055503.2A patent/CN104902989B/en not_active Expired - Fee Related
- 2013-10-14 US US14/436,604 patent/US10065157B2/en not_active Expired - Fee Related
- 2013-10-14 EP EP13784073.2A patent/EP2911773B1/en not_active Not-in-force
Patent Citations (258)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2630461A (en) | 1953-03-03 | Production of acetylene by incom | ||
US1504443A (en) | 1923-08-25 | 1924-08-12 | James W Gibbons | Paint-spraying apparatus |
US2119484A (en) | 1935-05-06 | 1938-05-31 | Du Pont | Chlorination of propylene dichloride |
GB471187A (en) | 1936-02-28 | 1937-08-30 | Du Pont | Improvements in or relating to the manufacture of chlorinated hydrocarbons |
GB471188A (en) | 1936-02-28 | 1937-08-30 | Du Pont | Improvements in or relating to the manufacture of chlorinated hydrocarbons |
GB471186A (en) | 1936-02-28 | 1937-08-30 | Du Pont | Improvements in or relating to the manufacture of chlorine derivatives of unsaturated hydrocarbons |
US2179378A (en) | 1936-07-18 | 1939-11-07 | Air Reduction | Production of acetylene |
US2207193A (en) | 1937-09-14 | 1940-07-09 | Shell Dev | Production of allyl type halides |
US2299441A (en) | 1939-09-02 | 1942-10-20 | Shell Dev | Catalytic halo-substitution of saturated organic compounds |
US2302228A (en) | 1940-04-02 | 1942-11-17 | Du Pont | Method of chlorination with sulphuryl chloride and production of monochloro-trimethyl acetic acid |
US2370342A (en) | 1940-04-30 | 1945-02-27 | Tide Water Associated Oil Comp | Halogenation |
US2378859A (en) | 1941-08-08 | 1945-06-19 | Distillers Co Yeast Ltd | Splitting-off of hydrogen halide from halogenated hydrocarbons |
US2379551A (en) * | 1944-04-27 | 1945-07-03 | Talley Henry Alfred Ernest | Apparatus for mixing gases |
US2449286A (en) | 1945-07-16 | 1948-09-14 | Shell Dev | Production of 1, 3-dihalopropylenes |
US2435983A (en) | 1945-12-01 | 1948-02-17 | Universal Oil Prod Co | Production of liquid hydrocarbons |
US2588867A (en) | 1948-10-25 | 1952-03-11 | Dow Chemical Co | Pyrolytic production of chlorohydrocarbons |
US2688592A (en) | 1950-10-21 | 1954-09-07 | Diamond Alkali Co | Photochemical process for preparing carbon tetrachloride |
DE857955C (en) | 1951-03-23 | 1952-12-04 | Basf Ag | Process for the production of tetrachlorethylene in addition to carbon tetrachloride |
US2762611A (en) | 1952-02-28 | 1956-09-11 | Pfaudler Co Inc | Tubular heat exchangers |
US2765359A (en) | 1953-02-10 | 1956-10-02 | Hydrocarbon Research Inc | Production of acetylene |
GB857086A (en) | 1956-08-30 | 1960-12-29 | Hoechst Ag | Process for the manufacture of carbon tetrachloride |
US3000980A (en) | 1958-04-07 | 1961-09-19 | Dow Chemical Co | Preparation of alkyl bromides |
US2973393A (en) | 1958-10-02 | 1961-02-28 | Dow Chemical Co | Chlorination of acetylenes |
US2964579A (en) | 1958-10-09 | 1960-12-13 | Houdry Process Corp | Selective hydrogenation of diolefins with copper chromite catalyst |
US3094567A (en) | 1960-02-25 | 1963-06-18 | Monsanto Chemicals | Chlorination of propynes |
US3112988A (en) | 1960-02-26 | 1963-12-03 | Sheil Oil Company | Mixing gases at supersonic velocity |
US3819731A (en) | 1960-03-23 | 1974-06-25 | Stauffer Chemical Co | Production of chlorinated unsaturated hydrocarbons |
US3651019A (en) | 1961-09-28 | 1972-03-21 | Yeda Res & Dev | Production of adducts of carbon tetrachloride or chloroform with olefinically unsaturated substances |
US3446859A (en) | 1962-06-11 | 1969-05-27 | Hooker Chemical Corp | Vapor phase condensation process |
US3502734A (en) | 1966-05-11 | 1970-03-24 | Du Pont | Process for partially chlorinating methyl chloride and/or methylene chloride |
LU52247A1 (en) | 1966-06-07 | 1966-12-28 | ||
GB1134585A (en) | 1966-07-22 | 1968-11-27 | Knapsack Ag | Process for the joint manufacture of 2,2,3-trichlorobutane and 1,2,3-trichlorobutane |
US3444263A (en) | 1966-11-09 | 1969-05-13 | Gulf Research Development Co | Method for converting ethylene to alpha olefins in the presence of an organic sulfide |
US3525595A (en) | 1967-05-19 | 1970-08-25 | Bayer Ag | Concentric cross flow nozzle apparatus for carrying out reactions between gases |
FR1546709A (en) | 1967-10-10 | 1968-11-22 | Mini Ind Chimice | Method and apparatus for the continuous system manufacture of hydrocarbon nitroso-derivatives |
US3558438A (en) | 1968-10-30 | 1971-01-26 | Du Pont | Distillation process and apparatus |
US3551512A (en) | 1968-11-01 | 1970-12-29 | Diamond Shamrock Corp | Pressure process for preparing acetylene |
US3676508A (en) | 1969-01-30 | 1972-07-11 | Hornig Anneliese | Process for the manufacture of carbon tetrachloride |
US3615202A (en) * | 1969-11-28 | 1971-10-26 | David R Stern | Process for the manufacture of titanium dioxide |
US4513154A (en) | 1971-07-30 | 1985-04-23 | Allied Corporation | Process for consecutive competitive gas phase reaction |
GB1548277A (en) | 1971-07-30 | 1979-07-11 | Allied Chem | Process for chlorination of hydrocarbons |
US3920757A (en) | 1971-08-25 | 1975-11-18 | Dow Chemical Co | Chlorination with sulfuryl chloride |
GB1381619A (en) | 1971-12-17 | 1975-01-22 | Monsanto Co | Process for the production of 1,2,3-trichloropropene |
US3926758A (en) | 1971-12-27 | 1975-12-16 | Monsanto Co | Preparation of 1,1,2,3-tetrachloropropene from 2,3-trichloropropane |
US3823195A (en) | 1971-12-27 | 1974-07-09 | Monsanto Co | Preparation of 1,1,2,3-tetrachloropropene from 1,2,3-trichloropropane |
US3954410A (en) | 1972-11-21 | 1976-05-04 | Merck Patent Gesellschaft Mit Beschraenkter Haftung | Solvents for NMR spectroscopy |
CH609022A5 (en) | 1973-06-12 | 1979-02-15 | Monsanto Co | Process for the preparation of 1,2,3-trichloropropene from 1,2,3-trichloropropane |
US3948858A (en) | 1973-09-22 | 1976-04-06 | Akzo N.V. | Polymerization of ethylenically unsaturated compounds |
US3872664A (en) | 1973-10-15 | 1975-03-25 | United Aircraft Corp | Swirl combustor with vortex burning and mixing |
US4145187A (en) * | 1974-03-21 | 1979-03-20 | Matthey Rustenburg Refiners (Pty.) Ltd. | Treatment of material with hydrogen chloride |
US3914167A (en) | 1974-08-26 | 1975-10-21 | Dow Chemical Co | Process for making cis-1,3-dichloropropene |
US4043766A (en) * | 1975-11-20 | 1977-08-23 | Dr. C. Otto & Comp. G.M.B.H. | Slag bath generator |
US4051182A (en) | 1976-04-12 | 1977-09-27 | Stauffer Chemical Company | Process for the manufacture of α-chloropropionyl chloride |
US4038372A (en) | 1976-05-05 | 1977-07-26 | The United States Of America As Represented By The Secretary Of The Navy | Process for manufacturing chloramine |
US4319062A (en) | 1976-08-02 | 1982-03-09 | The Dow Chemical Company | Allyl chloride process |
US4046656A (en) | 1976-12-06 | 1977-09-06 | The Dow Chemical Company | Photochlorination process for methyl aromatic compounds |
JPS544869A (en) | 1977-06-15 | 1979-01-13 | Babcock Hitachi Kk | Mixer for reducing agent and diluting agent |
JPS5479207A (en) | 1977-12-05 | 1979-06-25 | Showa Denko Kk | Preparation of 1,3-dichloropropene |
JPS54135712A (en) | 1978-04-13 | 1979-10-22 | Osaka Soda Co Ltd | Prepartion of 3-chloropropene |
SU899523A1 (en) | 1979-07-03 | 1982-01-23 | Уфимский Нефтяной Институт | Process for producing 1,1,2,3-tetrachloropropene |
US4381187A (en) * | 1980-03-24 | 1983-04-26 | United Technologies Corporation | Process for gasifying liquid hydrocarbon fuels |
WO1982001728A1 (en) | 1980-11-17 | 1982-05-27 | Manders Petrus G | A method for conveying a flexible thread by means of a pressurized gas |
US4550752A (en) * | 1980-11-17 | 1985-11-05 | Ruti-Te Strake B.V. | Method for conveying a flexible thread by means of pressurized gas |
EP0164798A1 (en) | 1981-09-01 | 1985-12-18 | George Andrew Olah | Process for the preparation of methyl monohalides |
DD209184A1 (en) | 1982-07-02 | 1984-04-25 | Buna Chem Werke Veb | PROCESS FOR THE PREPARATION OF CHLOROPROPENES |
US4650914A (en) | 1983-07-06 | 1987-03-17 | Monsanto Company | Process for producing 1,1,2,3-tetrachloropropene |
US4535194A (en) | 1983-07-06 | 1985-08-13 | Monsanto Co. | Process for producing 1,1,2,3-tetrachloropropene |
US4902393A (en) | 1983-08-25 | 1990-02-20 | Huels Aktiengesellschaft | Process for the production of 1,1,2-trichloro-2-methylpropane |
US4716255A (en) | 1983-08-25 | 1987-12-29 | Huels Aktiengesellschaft | Process for the production of 3,3-dichloro-2-methylpropene |
US4702809A (en) | 1984-04-25 | 1987-10-27 | Huels Aktiengesellschaft | Process for the production of 1,2,3-trichloro-2-methylpropane |
US4661648A (en) | 1984-08-20 | 1987-04-28 | Solvay & Cie (Societe Anonyme) | Process for carrying out substitution chlorination reactions of organic compounds by means of molecular chlorine in the presence of a chlorinated product serving as a radical initiator, and radical initiators used in such a process |
US4714792A (en) | 1984-09-06 | 1987-12-22 | Huels Aktiengesellschaft | Process for the production of 1,2,3-trichloropropane |
DD235631A1 (en) | 1985-03-25 | 1986-05-14 | Buna Chem Werke Veb | PROCESS FOR THE PREPARATION OF CHLOROPROPENES FROM 1,2-DICHLORPROPANE |
US4614572A (en) | 1985-07-08 | 1986-09-30 | The Dow Chemical Company | Liquid phase chlorination of chlorinated methanes |
US4726686A (en) | 1985-07-30 | 1988-02-23 | Hartmut Wolf | Swirl chamber |
US4644907A (en) | 1985-11-29 | 1987-02-24 | Hunter Edward H | Boiler tubes of enhanced efficiency and method of producing same |
US4727181A (en) | 1986-04-21 | 1988-02-23 | The Dow Chemical Company | Process for the preparation of α-halocinnamate esters |
US4849554A (en) | 1987-04-10 | 1989-07-18 | Imperial Chemical Industries Plc | Production of tetrafluoroethylene and hexafluoropropylene |
US5246903A (en) | 1987-05-26 | 1993-09-21 | The Dow Chemical Company | Process and catalyst for the dehydrohalogenation of halogenated hydrocarbons or alkylene halohydrins |
US4894205A (en) | 1987-09-18 | 1990-01-16 | Shell Oil Company | Multitube reactor |
US5132473A (en) | 1988-05-17 | 1992-07-21 | Daikin Industries, Ltd. | Process for production of 1,1,1-trifluoro-2,2-dichloroethane |
US5171899A (en) | 1988-05-17 | 1992-12-15 | Daikin Industries Ltd. | Process for production of 1,1,1-trifluoro-2,2-dichloroethane |
US5315044A (en) | 1988-05-17 | 1994-05-24 | Daikin Industries Ltd. | Process for production of 1,1,1-trifluoro-2,2-dichloroethane |
US4999102A (en) | 1988-12-16 | 1991-03-12 | The Amalgamated Sugar Company | Liquid transfer manifold system for maintaining plug flow |
US5254771A (en) | 1989-07-14 | 1993-10-19 | Hoechst Aktiengesellschaft | Process for the preparation of 1,1,1-trifluoro-2-2-dichloroethane under elevated pressure |
US5057634A (en) | 1989-12-19 | 1991-10-15 | E. I. Du Pont De Nemours And Company | Multistep synthesis of hexafluoropropylene |
US5178844A (en) | 1990-04-03 | 1993-01-12 | Phillips Petroleum Company | Method and apparatus for producing nitride products |
EP0453818A1 (en) | 1990-04-13 | 1991-10-30 | Ec Erdölchemie Gmbh | Process for the reductive dehalogenation of halogenated hydrocarbons and halogenated ethers |
US5254772A (en) | 1991-03-12 | 1993-10-19 | Imperial Chemical Industries Plc | Chemical process |
US5254788A (en) | 1991-09-10 | 1993-10-19 | Stone And Webster Engineering Corporation | Process for the production of olefins from light paraffins |
US5262575A (en) | 1992-08-04 | 1993-11-16 | The Dow Chemical Company | Production of allylic chlorides |
US5367105A (en) | 1992-10-23 | 1994-11-22 | Tokuyama Corporation | Process and device for production of allyl chloride |
US6229057B1 (en) | 1993-07-26 | 2001-05-08 | Zeneca Limited | Chlorination process |
US5414166A (en) | 1993-11-29 | 1995-05-09 | Korea Institute Of Science And Technology | Process for the preparation of 1,1,1-trifluoro-2,2-dichloroethane |
JPH08119885A (en) | 1994-10-25 | 1996-05-14 | Central Glass Co Ltd | Production of fluorinated hydrocarbon |
US5504266A (en) | 1995-05-24 | 1996-04-02 | The Dow Chemical Company | Process to make allyl chloride and reactor useful in that process |
EP1018366A2 (en) | 1995-05-24 | 2000-07-12 | The Dow Chemical Company | Spherical, egg-shaped or oval reactor |
US5684219A (en) | 1995-08-28 | 1997-11-04 | Laroche Industries Inc. | Process for preparing fluorinated aliphatic compounds |
US6235951B1 (en) | 1996-01-17 | 2001-05-22 | Central Glass Company, Limited | Method for producing 1,1,1,3,3-pentafluoropropane |
US5689020A (en) | 1996-03-11 | 1997-11-18 | Laroche Industries Inc. | High temperature chlorination process for the preparation of polychloroolefins |
US6111150A (en) | 1996-06-20 | 2000-08-29 | Central Glass Company, Limited | Method for producing 1,1,1,3,3,-pentafluoropropane |
US6538167B1 (en) | 1996-10-02 | 2003-03-25 | Exxonmobil Chemical Patents Inc. | Process for producing light olefins |
US5986151A (en) | 1997-02-05 | 1999-11-16 | Alliedsignal Inc. | Fluorinated propenes from pentafluoropropane |
US5811605A (en) | 1997-02-19 | 1998-09-22 | Ppg Industries, Inc. | Preparation of 1,2,3,3-tetrachloropropene |
WO1999006314A1 (en) | 1997-07-31 | 1999-02-11 | E.I. Du Pont De Nemours And Company | Air jet piddling |
US5895825A (en) | 1997-12-01 | 1999-04-20 | Elf Atochem North America, Inc. | Preparation of 1,1,1,3,3-pentafluoropropane |
US6160187A (en) | 1997-12-18 | 2000-12-12 | The Dow Chemical Company | Method for making glycol in an adiabatic reactor system |
US6472573B1 (en) | 1998-03-23 | 2002-10-29 | Daikin Industries, Ltd. | Process for producing 1,1,1,3,3-pentafluoropropane |
US6187976B1 (en) | 1998-04-09 | 2001-02-13 | Alliedsignal Inc. | Process for the preparation of fluorine containing hydrohalocarbons |
US6545176B1 (en) | 1998-11-04 | 2003-04-08 | Rohm And Haas Company | Apparatus and process for the high yield production of methyl methacrylate or methacrylic acid |
US6610177B2 (en) | 1998-11-04 | 2003-08-26 | Rohm And Haas Company | Apparatus and process for the high yield production of methyl methacrylate or methacrylic acid |
US20010018962A1 (en) | 1998-12-23 | 2001-09-06 | American Air Liquide Inc. | Heat exchanger for preheating an oxidizing gas |
US7226567B1 (en) | 1999-03-16 | 2007-06-05 | Basf Aktiengesellschaft | Multi-tube fixed-bed reactor, especially for catalytic gas phase reactions |
US6958135B1 (en) | 1999-06-15 | 2005-10-25 | Methanol Casale S.A. | Isothermal reactor for exothermic or endothermic heterogeneous reactions |
US7282120B2 (en) | 1999-06-16 | 2007-10-16 | Solvay Fluor Gmbh | UV-activated chlorination process |
EP1097984A2 (en) | 1999-11-02 | 2001-05-09 | Noell-KRC Energie- und Umwelttechnik GmbH | Process and plant for the cooling and cleaning of gasification gases |
JP2001151708A (en) | 1999-11-22 | 2001-06-05 | Central Glass Co Ltd | Method for producing 1,1,1,3,3-pentachloropropane |
WO2001038275A1 (en) | 1999-11-22 | 2001-05-31 | The Dow Chemical Company | Dehydrohalogenation of halogenated alkanes using rare earth halide or oxyhalide catalyst |
WO2001038271A1 (en) | 1999-11-22 | 2001-05-31 | The Dow Chemical Company | Oxyhalogenation process using catalyst having porous rare earth halide support |
US6118018A (en) | 1999-12-06 | 2000-09-12 | Occidental Chemical Corporation | Chlorination and bromination of aromatic compounds at atmospheric pressure |
JP2001213820A (en) | 2000-01-31 | 2001-08-07 | Central Glass Co Ltd | Method of producing 1,1,1,3,3-pentachloro-propane |
US6613127B1 (en) | 2000-05-05 | 2003-09-02 | Dow Global Technologies Inc. | Quench apparatus and method for the reformation of organic materials |
US20020110711A1 (en) | 2000-11-04 | 2002-08-15 | Stefan Boneberg | Method and device for starting a reacator in a gas-generating system |
US6518467B2 (en) | 2000-12-29 | 2003-02-11 | Honeywell International Inc. | Method of making hydrofluorocarbons and hydrochlorofluorocarbons |
US20020087039A1 (en) | 2000-12-29 | 2002-07-04 | Tung Hsueh Sung | Method of making hydrofluorocarbons and hydrochlorofluorocarbons |
US6551469B1 (en) | 2001-11-27 | 2003-04-22 | Honeywell International | Photochlorination of 1,1,1,3,3-pentafluoropropane |
US7297814B2 (en) | 2002-01-11 | 2007-11-20 | Mitsubishi Chemical Corporation | Multitube reactor, vapor phase catalytic oxidation method using the multitube reactor, and start up method applied to the multitube reactor |
US7117934B2 (en) | 2002-03-15 | 2006-10-10 | H2Gen Innovations, Inc. | Method and apparatus for minimizing adverse effects of thermal expansion in a heat exchange reactor |
US7172733B2 (en) * | 2002-05-06 | 2007-02-06 | Institut Francais Du Petrole | Device for injection of hydrocarbons into a fluidized chamber |
US6924403B2 (en) | 2002-06-26 | 2005-08-02 | E. I. Du Pont De Nemours And Company | Synthesis of hexafluoropropylene |
US6683216B1 (en) | 2002-11-06 | 2004-01-27 | Eastman Chemical Company | Continuous process for the preparation of amines |
US20060150445A1 (en) | 2003-01-24 | 2006-07-13 | Redding John H | Underwater sediment management |
US7521029B2 (en) | 2003-01-31 | 2009-04-21 | Man Dwe Gmbh | Shell-and-tube type reactor for carrying out catalytic gaseous phase reactions and a procedure for operating the same |
US7378559B2 (en) | 2003-03-07 | 2008-05-27 | Dow Global Technologies Inc. | Continuous process and system of producing polyether polyols |
US7140558B2 (en) * | 2003-03-24 | 2006-11-28 | Irene Base, legal representative | Mixing arrangement for atomizing nozzle in multi-phase flow |
US7588739B2 (en) | 2003-07-14 | 2009-09-15 | Mitsubishi Rayon Co., Ltd. | Fixed bed multitube reactor |
US20060292046A1 (en) | 2003-07-31 | 2006-12-28 | Dow Global Technologies Inc. | Oxidation process and reactor with modified feed system |
WO2005016509A1 (en) | 2003-07-31 | 2005-02-24 | Dow Global Technologies Inc. | Oxidation process and reactor with modified feed system |
US6825383B1 (en) | 2003-09-22 | 2004-11-30 | Council Of Scientific And Industrial Research | Catalytic process for regiospecific chlorination of alkanes, alkenes and arenes |
US7714177B2 (en) | 2004-04-29 | 2010-05-11 | Honeywell International Inc. | Processes for synthesis of 1,3,3,3-tetrafluoropropene |
US7345209B2 (en) | 2004-04-29 | 2008-03-18 | Honeywell International Inc. | Processes for synthesis of 1,3,3,3-tetrafluoropropene |
US20070197842A1 (en) | 2004-04-29 | 2007-08-23 | Honeywell International Inc. | Method for producing fluorinated organic compounds |
US7951982B2 (en) | 2004-04-29 | 2011-05-31 | Honeywell International Inc. | Method for producing fluorinated organic compounds |
US7880040B2 (en) | 2004-04-29 | 2011-02-01 | Honeywell International Inc. | Method for producing fluorinated organic compounds |
US7189884B2 (en) | 2004-04-29 | 2007-03-13 | Honeywell International | Processes for synthesis of tetrafluoropropene |
US8084653B2 (en) | 2004-04-29 | 2011-12-27 | Honeywell International, Inc. | Method for producing fluorinated organic compounds |
US8395000B2 (en) | 2004-04-29 | 2013-03-12 | Honeywell International Inc. | Method for producing fluorinated organic compounds |
US8383867B2 (en) | 2004-04-29 | 2013-02-26 | Honeywell International Inc. | Method for producing fluorinated organic compounds |
US20070197841A1 (en) | 2004-04-29 | 2007-08-23 | Honeywell International Inc. | Method for producing fluorinated organic compounds |
US7674939B2 (en) | 2004-04-29 | 2010-03-09 | Honeywell International Inc. | Method for producing fluorinated organic compounds |
US7659434B2 (en) | 2004-04-29 | 2010-02-09 | Honeywell International Inc. | Method for producing fluorinated organic compounds |
US8058486B2 (en) | 2004-04-29 | 2011-11-15 | Honeywell International Inc. | Integrated process to produce 2,3,3,3-tetrafluoropropene |
US7371904B2 (en) | 2004-04-29 | 2008-05-13 | Honeywell International Inc. | Processes for synthesis of 1,3,3,3-tetrafluoropropene |
US20080021229A1 (en) | 2004-05-21 | 2008-01-24 | Maughon Bob R | Process for Preparing Epichlorhydrin from Ethane |
US20080118018A1 (en) | 2004-12-10 | 2008-05-22 | Schrauwen Franciscus Johannes | Reactor Tube Apparatus |
US20070265368A1 (en) | 2004-12-22 | 2007-11-15 | Velliyur Nott Mallikarjuna Rao | Functionalized Copolymers of Terminally Functionalized Perfluoro (Alkyl Vinyl Ether) Reactor Wall for Photochemical Reactions, Process for Increasing Fluorine Content in Hydrocaebons and Halohydrocarbons and Olefin Production |
US20070259296A1 (en) * | 2004-12-23 | 2007-11-08 | Knoepfel Hans P | Premix Burner With Mixing Section |
JP2006272267A (en) | 2005-03-30 | 2006-10-12 | Fuji Photo Film Co Ltd | Method of operating microchemical device |
US7396965B2 (en) | 2005-05-12 | 2008-07-08 | Honeywell International Inc. | Method for producing fluorinated organic compounds |
US7511101B2 (en) | 2005-05-13 | 2009-03-31 | Fina Technology, Inc. | Plug flow reactor and polymers prepared therewith |
JP2007021396A (en) | 2005-07-19 | 2007-02-01 | Japan Science & Technology Agency | Method for removing heavy metal |
US8123398B2 (en) | 2005-08-09 | 2012-02-28 | Canon Kabushiki Kaisha | Fluid-processing device |
DE102005044501A1 (en) | 2005-09-16 | 2007-03-22 | Roquette, Eberhard, Dipl.-Ing. | Preparation of ester containing alcohol and fatty acid by nozzle system (venturi principle) comprising nozzle fitter or holder, mixing tube, diffuser and two chamber mixing system |
US8071825B2 (en) | 2006-01-03 | 2011-12-06 | Honeywell International Inc. | Method for producing fluorinated organic compounds |
WO2007079435A2 (en) | 2006-01-03 | 2007-07-12 | Honeywell International Inc. | Method for producing fluorinated organic compounds |
WO2007079431A2 (en) | 2006-01-03 | 2007-07-12 | Honeywell International Inc. | Method for producing fluorinated organic compounds |
US7695695B2 (en) | 2006-01-18 | 2010-04-13 | Lg Chem, Ltd. | Reactor or heat exchanger with improved heat transfer performance |
WO2007096383A1 (en) | 2006-02-21 | 2007-08-30 | Sachtleben Chemie Gmbh | Method for carrying out chemical and physical processes and reaction cells |
US7687670B2 (en) | 2006-03-31 | 2010-03-30 | E.I. Du Pont De Nemours And Company | Coproduction of hydrofluoroolefins |
US7836941B2 (en) | 2006-05-19 | 2010-11-23 | Exxonmobil Research And Engineering Company | Mitigation of in-tube fouling in heat exchangers using controlled mechanical vibration |
US20080073063A1 (en) | 2006-06-23 | 2008-03-27 | Exxonmobil Research And Engineering Company | Reduction of fouling in heat exchangers |
US20090270568A1 (en) | 2006-06-26 | 2009-10-29 | Solvay (Société Anonyme) | Process for the Manufacture of 1,2-Dichloroethane |
US8058490B2 (en) | 2006-06-26 | 2011-11-15 | Solvay (Societé Anonyme) | Process for the manufacture of 1,2-dichloroethane |
JP2008063314A (en) | 2006-09-04 | 2008-03-21 | Tokyo Kasei Kogyo Kk | Environment-conscious hypervalent iodine reagent |
US8232435B2 (en) | 2006-09-05 | 2012-07-31 | E I Du Pont De Nemours And Company | 1,2,3,3,3-pentafluoropropene production processes |
US20090088547A1 (en) | 2006-10-17 | 2009-04-02 | Rpo Pty Limited | Process for producing polysiloxanes and use of the same |
WO2008054781A1 (en) | 2006-10-31 | 2008-05-08 | E. I. Du Pont De Nemours And Company | Processes for the production of fluoropropanes and halopropenes and azeotropic compositions of 2-chloro-3,3,3-trifluoro-1-propene with hf and of 1,1,1,2,2-pentafluoropropane with hf |
US8398882B2 (en) | 2006-10-31 | 2013-03-19 | E I Du Pont De Nemours And Company | Processes for the production of fluoropropanes and halopropenes and azeotropic compositions of 2-chloro-3,3,3-trifluoro-1-propene with HF and of 1,1,1,2,2-pentafluoropropane with HF |
US20080207962A1 (en) | 2007-02-23 | 2008-08-28 | Velliyur Nott Mallikarjuna Rao | Compositions containing chromium, oxygen, and at least two modifier metals selected the group consisting of gold, silver, and palladium, their preparation, and their use as catalysts and catalyst precursors |
US20100041864A1 (en) | 2007-04-10 | 2010-02-18 | Asahi Glass Company, Limited | Double metal cyanide complex catalyst having organic ligand, process for its production and method for producing polyether polyol |
JP2009000592A (en) | 2007-06-19 | 2009-01-08 | Hitachi Ltd | Reactor and reaction system |
US8076521B2 (en) | 2007-06-27 | 2011-12-13 | Arkema Inc. | Process for the manufacture of hydrofluoroolefins |
US20100185029A1 (en) | 2007-06-27 | 2010-07-22 | Arkema Inc. | Two step process for the manufacture of hydrofluoroolefins |
US20090018377A1 (en) | 2007-07-09 | 2009-01-15 | Boyce C Bradford | Catalytic process for the preparation of fluorinated halocarbons |
JP2009046653A (en) | 2007-07-24 | 2009-03-05 | Nagase Chemtex Corp | Method for producing polymer of aromatic compound and heterocyclic aromatic compound by using hypervalent iodine reagent |
US20090030249A1 (en) | 2007-07-25 | 2009-01-29 | Honeywell International Inc. | Processes for preparing 1,1,2,3-tetrachloropropene |
US8258355B2 (en) | 2007-07-25 | 2012-09-04 | Honeywell International Inc. | Processes for preparing 1,1,2,3-tetrachloropropene |
WO2009015304A1 (en) | 2007-07-25 | 2009-01-29 | Honeywell International Inc. | Processes for preparing 1,1,2,3-tetrachloropropene |
CN101754941A (en) | 2007-07-25 | 2010-06-23 | 霍尼韦尔国际公司 | Processes for preparing 1,1,2,3-tetrachloropropene |
US20090203945A1 (en) | 2007-08-22 | 2009-08-13 | Honeywell International Inc. | Method for producing fluorinated organic compounds |
US20100263278A1 (en) | 2007-09-18 | 2010-10-21 | Uhde Gmbh | Gasification reactor and process for entrained-flow gasification |
US8367867B2 (en) | 2007-10-04 | 2013-02-05 | Urea Casale S.A. | Process and plant for urea production |
US20090099396A1 (en) | 2007-10-15 | 2009-04-16 | Honeywell International Inc. | Process for synthesis of fluorinated olefins |
US20090117014A1 (en) | 2007-11-06 | 2009-05-07 | Quantumsphere, Inc. | System and method for ammonia synthesis |
WO2009067571A1 (en) | 2007-11-20 | 2009-05-28 | E. I. Du Pont De Nemours And Company | Synthesis of hydrofluoroalkanols and hydrofluoroalkenes |
US8487146B2 (en) | 2007-12-19 | 2013-07-16 | Occidental Chemical Corporation | Methods of making chlorinated hydrocarbons |
US8115038B2 (en) | 2007-12-19 | 2012-02-14 | Occidental Chemical Corporation | Methods of making chlorinated hydrocarbons |
US8614363B2 (en) | 2007-12-19 | 2013-12-24 | Occidental Chemical Corporation | Methods of making chlorinated hydrocarbons |
WO2009087423A1 (en) | 2008-01-11 | 2009-07-16 | John Redding | Improvements in or relating to jet nozzles |
CN101215220A (en) | 2008-01-16 | 2008-07-09 | 西安近代化学研究所 | Preparation method for 1,1,1,3-tetrafluoropropene |
CN101597209A (en) | 2008-03-20 | 2009-12-09 | 霍尼韦尔国际公司 | Be used to prepare 2,3,3, the integrated process of 3-tetrafluoeopropene |
US8071826B2 (en) | 2008-04-04 | 2011-12-06 | Honeywell International Inc. | Process for the preparation of 2,3,3,3-tetrafluoropropene (HFO-1234yf) |
US20110251425A1 (en) | 2008-08-07 | 2011-10-13 | Basf Se | Process for preparing aromatic isocyanates |
US20110172472A1 (en) | 2008-09-25 | 2011-07-14 | Central Glass Company, Limited | Process for Producing 1,3,3,3-Tetrafluoropropene |
US8258353B2 (en) | 2008-10-13 | 2012-09-04 | Dow Global Technologies, Llc | Process for the production of chlorinated and/or fluorinated propenes |
US20110218369A1 (en) | 2008-11-19 | 2011-09-08 | Arkema Inc. | Process for the manufacture of hydrofluoroolefins |
US8357828B2 (en) | 2008-12-25 | 2013-01-22 | Asahi Glass Company, Limited | Processes for producing 1,1-dichloro-2,3,3,3-tetrafluoropropene and 2,3,3,3-tetrafluoropropene |
CN101492341A (en) | 2009-03-05 | 2009-07-29 | 杨海珍 | Process for producing saturated polychloralkane |
US8614361B2 (en) | 2009-04-23 | 2013-12-24 | Daikin Industries, Ltd. | Process for preparation of 2,3,3,3-tetrafluoropropene |
CN101544535A (en) | 2009-05-01 | 2009-09-30 | 浙江三美化工股份有限公司 | Method for preparing synthetic 1,1,1,3,3-pentachloro propane |
US20120065434A1 (en) | 2009-05-13 | 2012-03-15 | Masatoshi Nose | Process for preparing chlorine-containing fluorocarbon compound |
US8581011B2 (en) | 2009-10-09 | 2013-11-12 | Dow Global Technologies, Llc | Process for the production of chlorinated and/or fluorinated propenes |
US8558041B2 (en) | 2009-10-09 | 2013-10-15 | Dow Global Technologies, Llc | Isothermal multitube reactors and processes incorporating the same |
US8581012B2 (en) | 2009-10-09 | 2013-11-12 | Dow Global Technologies, Llc | Processes for the production of chlorinated and/or fluorinated propenes and higher alkenes |
US20110087056A1 (en) | 2009-10-09 | 2011-04-14 | Dow Global Technologies | Adiabatic plug flow reactors and processes incorporating the same |
US8926918B2 (en) | 2009-10-09 | 2015-01-06 | Dow Global Technologies Llc | Isothermal multitube reactors |
US8933280B2 (en) | 2009-10-09 | 2015-01-13 | Dow Global Technologies Llc | Processes for the production of hydrofluoroolefins |
WO2011060211A1 (en) | 2009-11-16 | 2011-05-19 | Arkema Inc. | Method to purify and stabilize chloroolefins |
WO2011065574A1 (en) | 2009-11-27 | 2011-06-03 | Daikin Industries, Ltd. | Process for preparing 1,1,2,3-tetrachloropropene |
US8158836B2 (en) | 2009-12-23 | 2012-04-17 | Arkema France | Catalytic gas phase fluorination of 1230xa to 1234yf |
US20110155942A1 (en) | 2009-12-23 | 2011-06-30 | Arkema France | Catalytic Gas Phase Fluorination of 1230xa to 1234yf |
JP2011144148A (en) | 2010-01-18 | 2011-07-28 | Nippon Zeon Co Ltd | Hydrogen-containing halogenated cyclopentane, and method for producing heptafluorocyclopentene |
CN101955414A (en) | 2010-04-20 | 2011-01-26 | 南通泰禾化工有限公司 | Technology for preparing 1, 1, 2, 3-tetrachloropropene |
DE102010022414A1 (en) | 2010-06-01 | 2011-12-01 | Günther Kramb jun. | Emulsifying device for emulsifying two or multiple substances used in beverage industry, chemical industry, pharmaceutical industry and medicines, has housing which encloses reaction chamber that has inlets for both mediums |
WO2012011844A1 (en) | 2010-07-21 | 2012-01-26 | Открытое Акционерное Общество "Научно-Исследовательский И Проектный Институт Карбамида И Продуктов Органического Синтеза" (Оао Ниик) | Gas-liquid reactor (variant embodiments) |
CN101913980A (en) | 2010-09-07 | 2010-12-15 | 西安近代化学研究所 | Production method of 1,1,1,3,3-pentachloropropane |
CN101913979A (en) | 2010-09-07 | 2010-12-15 | 西安近代化学研究所 | Production method of 1,1,1,3,3-pentachlorobutane |
CN101982227A (en) | 2010-09-15 | 2011-03-02 | 山东东岳高分子材料有限公司 | Rapid gas hybrid reactor for high temperature cracking and application thereof |
CN102001911A (en) | 2010-09-20 | 2011-04-06 | 西安近代化学研究所 | Method for preparing 2,3,3,3-tetrafluoropropene |
WO2012081482A1 (en) | 2010-12-16 | 2012-06-21 | 株式会社トクヤマ | Method for producing c3 chlorinated hydrocarbon |
WO2012166394A1 (en) | 2011-05-31 | 2012-12-06 | Dow Global Technologies, Llc | Process for the production of chlorinated propenes |
WO2012166393A1 (en) | 2011-05-31 | 2012-12-06 | Dow Global Technologies, Llc | Process for the production of chlorinated propenes |
US9056808B2 (en) | 2011-05-31 | 2015-06-16 | Dow Global Technologies, Llc | Process for the production of chlorinated propenes |
CN102249846A (en) | 2011-05-31 | 2011-11-23 | 浙江师范大学 | Co-production preparation method of 2-chloro-3,3,3-trifluoropropene and 2,3-dichloro-1,1-difluoro propylene |
US20140081055A1 (en) | 2011-05-31 | 2014-03-20 | Dow Global Technologies, Llc | Process for the production of chlorinated propenes |
US8907148B2 (en) | 2011-08-07 | 2014-12-09 | Dow Global Technologies Llc | Process for the production of chlorinated propenes |
US20140163266A1 (en) | 2011-08-07 | 2014-06-12 | Dow Global Technologies Llc | Process for the production of chlorinated propenes |
US20140179962A1 (en) | 2011-08-07 | 2014-06-26 | Dow Global Technologies Llc | Process for the production of chlorinated propenes |
CN102351637A (en) | 2011-08-31 | 2012-02-15 | 浙江师范大学 | Method for preparing 2,3,3,3-tetrafluoropropene |
US9067855B2 (en) | 2011-11-21 | 2015-06-30 | Dow Global Technologies Llc | Process for the production of chlorinated alkanes |
US20150045592A1 (en) | 2011-11-21 | 2015-02-12 | Dow Global Technologies Llc | Process for the production of chlorinated alkanes |
WO2013082410A1 (en) | 2011-12-02 | 2013-06-06 | Dow Global Technologies, Llc | Process for the production of chlorinated alkanes |
US20140323776A1 (en) | 2011-12-02 | 2014-10-30 | Dow Global Technologies Llc | Process for the production of chlorinated alkanes |
US20140323775A1 (en) | 2011-12-02 | 2014-10-30 | Dow Global Technologies Llc | Process for the production of chlorinated alkanes |
US20140371494A1 (en) | 2011-12-13 | 2014-12-18 | Dow Global Technologies Llc | Process for the production of chlorinated propanes and propenes |
US20140336425A1 (en) | 2011-12-22 | 2014-11-13 | Dow Global Technologies Llc | Process for the production of tetrachloromethane |
US20140336431A1 (en) | 2011-12-23 | 2014-11-13 | Dow Global Technologies Llc | Process for the production of alkenes and/or aromatic compounds |
US20150057471A1 (en) | 2011-12-23 | 2015-02-26 | Dow Global Technologies Llc | Chlorinating agents |
US8957258B2 (en) | 2012-01-24 | 2015-02-17 | Kanto Denka Kogyo Co., Ltd. | BIS(1,1-Dichloro-3,3,3-trifluoropropyl) ether and process for preparing the same |
WO2014046977A1 (en) | 2012-09-20 | 2014-03-27 | Dow Global Technologies, Llc | Process for the production of chlorinated propenes |
WO2014046970A1 (en) | 2012-09-20 | 2014-03-27 | Dow Global Technologies, Llc | Process for the production of chlorinated propenes |
US20150217256A1 (en) | 2012-09-30 | 2015-08-06 | Dow Global Technologies Llc | Weir quench and processes incorporating the same |
WO2014066083A1 (en) | 2012-10-26 | 2014-05-01 | Dow Global Technologies, Llc | Mixer and reactor and process incorporating the same |
WO2014100066A1 (en) | 2012-12-18 | 2014-06-26 | Dow Global Technologies, Llc | Process for the production of chlorinated propenes |
WO2014100039A1 (en) | 2012-12-19 | 2014-06-26 | Dow Global Technologies, Llc | Process for the production of chlorinated propenes |
WO2014134233A2 (en) | 2013-02-27 | 2014-09-04 | Dow Global Technologies Llc | Process for the production of chlorinated propenes |
WO2014134377A2 (en) | 2013-02-28 | 2014-09-04 | Dow Global Technologies Llc | Process for the production of chlorinated propanes |
WO2014164368A1 (en) | 2013-03-09 | 2014-10-09 | Dow Global Technologies Llc | Process for the production of chlorinated alkanes |
Non-Patent Citations (45)
Also Published As
Publication number | Publication date |
---|---|
CN104902989B (en) | 2017-09-08 |
JP6363610B2 (en) | 2018-07-25 |
WO2014066083A1 (en) | 2014-05-01 |
CN104902989A (en) | 2015-09-09 |
CA2887559A1 (en) | 2014-05-01 |
EP2911773B1 (en) | 2017-10-04 |
JP2015536816A (en) | 2015-12-24 |
US20160158715A1 (en) | 2016-06-09 |
EP2911773A1 (en) | 2015-09-02 |
IN2015DN03949A (en) | 2015-10-02 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US10065157B2 (en) | Mixer and processes incorporating the same | |
CN102665890B (en) | The adiabatic plug flow reactor of production chlorination and/or fluorinated acrylamide and higher alkene and method | |
US9795941B2 (en) | Weir quench and processes incorporating the same | |
CN102596387B (en) | The isothermal multitubular reactor of production chlorination and/or fluorinated acrylamide and higher alkene and method | |
US9199899B2 (en) | Process for the production of chlorinated alkanes | |
KR20120084729A (en) | Process for the production of chlorinated and/or fluorinated propenes and higher alkenes | |
EP2782889A1 (en) | Process for the production of chlorinated alkanes | |
CN101133008A (en) | Non-catalytic manufacture of 1,1,3,3,3-pentafluoropropene from 1,1,1,3,3,3-hexafluoropropane | |
JP6908596B2 (en) | Method for producing C3 chlorinated alkane and alkene compound | |
CN104011000A (en) | Process For The Production Of Tetrachloromethane | |
JP2015529247A (en) | Process for the production of chlorinated propene | |
TW202216645A (en) | A process for producing highly pure chlorinated alkane | |
CN103717558A (en) | Process for production of chlorinated propenes | |
JP2023552168A (en) | reactor | |
CN111138292A (en) | Method for producing 1,1, 1-trifluoro-2-chloroethane and/or trifluoroethylamine | |
CN104125939A (en) | Process for reactor passivation | |
de Weerd | Process intensification: Choosing the right tools |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
AS | Assignment |
Owner name: DOW GLOBAL TECHNOLOGIES LLC, MICHIGAN Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNORS:TIRTOWIDJOJO, MAX M.;BAI, HUA;CALVERLEY, EDWARD M.;REEL/FRAME:035765/0535 Effective date: 20130109 |
|
AS | Assignment |
Owner name: DOW GLOBAL TECHNOLOGIES LLC, MICHIGAN Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNORS:TIRTOWIDJOJO, MAX M.;BAI, HUA;CALVERLEY, EDWARD M.;REEL/FRAME:036205/0041 Effective date: 20130109 |
|
AS | Assignment |
Owner name: BLUE CUBE IP LLC, MICHIGAN Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNOR:DOW GLOBAL TECHNOLOGIES LLC;REEL/FRAME:036254/0315 Effective date: 20150804 |
|
STCF | Information on status: patent grant |
Free format text: PATENTED CASE |
|
FEPP | Fee payment procedure |
Free format text: MAINTENANCE FEE REMINDER MAILED (ORIGINAL EVENT CODE: REM.); ENTITY STATUS OF PATENT OWNER: LARGE ENTITY |
|
LAPS | Lapse for failure to pay maintenance fees |
Free format text: PATENT EXPIRED FOR FAILURE TO PAY MAINTENANCE FEES (ORIGINAL EVENT CODE: EXP.); ENTITY STATUS OF PATENT OWNER: LARGE ENTITY |
|
STCH | Information on status: patent discontinuation |
Free format text: PATENT EXPIRED DUE TO NONPAYMENT OF MAINTENANCE FEES UNDER 37 CFR 1.362 |
|
FP | Lapsed due to failure to pay maintenance fee |
Effective date: 20220904 |